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NHLBI Next Gen - Coronary artery disease and myocardial infarction (Dr. Eric Topol, Scripps Research Institute)

NHLBI Next Gen - Coronary artery disease and myocardial infarction (Dr. Eric Topol, Scripps Research Institute)

Showing 33–48 of 97 results

Cell Line	Cell Line Alias	Cell Type	Disease	Genetic Alteration/Mutation	Sex	Age at Collection	Ethnicity	Genetically Related Cell Lines	dbGaP Data
SCRP0104i	KBET0104i	Human iPS	None reported	Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the risk alleles at all 3 sites.	Male	59 Years	Caucasian > European	No	No
SCRP0202i	KBET0202i	Human iPS	Coronary artery disease\|Myocardial infarction	Three sites within the 9p21 region were genotyped for each donor. This donor was heterozygous for the risk and non-risk alleles at all 3 sites.	Male	49 Years	Caucasian > European	No	No
SCRP0203i	C00096	Human iPS	Coronary artery disease	Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the non-risk alleles at all 3 sites.	Male	86 Years	Caucasian > European	No	No
SCRP0302i	C00103	Human iPS	Coronary artery disease	Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the risk alleles at all 3 sites.	Male	79 Years	Caucasian > European	No	No
SCRP0307i	KBET0307i	Human iPS	None reported	Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the non-risk alleles at all 3 sites.	Male	62 Years	Caucasian > European	No	No
SCRP0402i	KBET0402i	Human iPS	Coronary artery disease\|Myocardial infarction	Three sites within the 9p21 region were genotyped for each donor. This donor was heterozygous for the risk and non-risk alleles at all 3 sites.	Male	73 Years	Caucasian > European	No	No
SCRP0404i	C00125	Human iPS	Coronary artery disease	Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the risk alleles at all 3 sites.	Male	66 Years	Caucasian > European	No	No
SCRP0517i	KBET0517i	Human iPS	Coronary artery disease	Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the risk alleles at all 3 sites.	Male	57 Years	Caucasian > European	No	No
SCRP0601i	KBET0601i	Human iPS	Coronary artery disease\|Myocardial infarction	Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the risk alleles at all 3 sites.	Male	69 Years	Caucasian	No	No
SCRP0608i	C00168	Human iPS	Coronary artery disease\|Myocardial infarction	Three sites within the 9p21 region were genotyped for each donor. This donor was heterozygous for the risk and non-risk alleles at all 3 sites.	Male	70 Years	Caucasian > European	No	No

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