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Collection

Collection

Showing 1361–1376 of 1517 results

Cell Line	Cell Line Alias	Cell Type	Disease	Genetic Alteration/Mutation	Sex	Age at Collection	Ethnicity	Genetically Related Cell Lines	dbGaP Data
SCRP2706i	C00519	Human iPS	Coronary artery disease	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.	Female	76 Years	Caucasian	No	No
SCRP2801i	C00541	Human iPS	Coronary artery disease	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	65 Years	Caucasian > European	No	No
SCRP3202i	C00599	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	82 Years	Caucasian	No	No
SCRP3304i	C00611	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	86 Years	Caucasian	No	No
SCRP3401i	C00651	Human iPS	Coronary artery disease	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	68 Years	Caucasian	No	No
SCRP3510i	C00706	Human iPS	Coronary artery disease\|Myocardial infarction	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	68 Years	Caucasian	No	No
SCRP3601i	C00709	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	73 Years	Caucasian	No	No
SCRP3702i	C00710	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
SCRP3803i	C00711	Human iPS	Coronary artery disease\|Myocardial infarction	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	89 Years	Caucasian	No	No
SCRP3901i	C00717	Human iPS	Coronary artery disease	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.	Female	65 Years	Caucasian	No	No

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