rs1163662
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1163662(C;C) |
Make rs1163662(C;T) |
Make rs1163662(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 80898148 |
Gene | LIN7A |
is a | snp |
is | mentioned by |
dbSNP | rs1163662 |
dbSNP (classic) | rs1163662 |
ClinGen | rs1163662 |
ebi | rs1163662 |
HLI | rs1163662 |
Exac | rs1163662 |
Gnomad | rs1163662 |
Varsome | rs1163662 |
LitVar | rs1163662 |
Map | rs1163662 |
PheGenI | rs1163662 |
Biobank | rs1163662 |
1000 genomes | rs1163662 |
hgdp | rs1163662 |
ensembl | rs1163662 |
geneview | rs1163662 |
scholar | rs1163662 |
rs1163662 | |
pharmgkb | rs1163662 |
gwascentral | rs1163662 |
openSNP | rs1163662 |
23andMe | rs1163662 |
SNPshot | rs1163662 |
SNPdbe | rs1163662 |
MSV3d | rs1163662 |
GWAS Ctlg | rs1163662 |
GMAF | 0.3834 |
Max Magnitude | 0 |
[PMID 20227257] Polymorphisms in the platelet-specific collagen receptor GP6 are associated with risk of nonfatal myocardial infarction in Caucasians