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rs1324694

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1324694(C;T)
Make rs1324694(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position100186688
GeneERLIN1
is asnp
is mentioned by
dbSNPrs1324694
ebirs1324694
HLIrs1324694
Exacrs1324694
Varsomers1324694
Maprs1324694
PheGenIrs1324694
hapmaprs1324694
1000 genomesrs1324694
hgdprs1324694
ensemblrs1324694
gopubmedrs1324694
geneviewrs1324694
scholarrs1324694
googlers1324694
pharmgkbrs1324694
gwascentralrs1324694
openSNPrs1324694
23andMers1324694
23andMe allrs1324694
SNP Nexus

SNPshotrs1324694
SNPdbers1324694
MSV3drs1324694
GWAS Ctlgrs1324694
GMAF0.07254
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 20198315] Association of genetic variants with hemorrhagic stroke in Japanese individuals