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rs1163662

From SNPedia

Orientationminus
Stabilizedplus
Make rs1163662(C;C)
Make rs1163662(C;T)
Make rs1163662(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position80898148
GeneLIN7A
is asnp
is mentioned by
dbSNPrs1163662
ebirs1163662
HLIrs1163662
Exacrs1163662
Varsomers1163662
Maprs1163662
PheGenIrs1163662
hapmaprs1163662
1000 genomesrs1163662
hgdprs1163662
ensemblrs1163662
gopubmedrs1163662
geneviewrs1163662
scholarrs1163662
googlers1163662
pharmgkbrs1163662
gwascentralrs1163662
openSNPrs1163662
23andMers1163662
23andMe allrs1163662
SNP Nexus

SNPshotrs1163662
SNPdbers1163662
MSV3drs1163662
GWAS Ctlgrs1163662
GMAF0.3834
Max Magnitude

[PMID 20227257OA-icon.png] Polymorphisms in the platelet-specific collagen receptor GP6 are associated with risk of nonfatal myocardial infarction in Caucasians



GET Evidence
rs1163662
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.567797
summary