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rs6960920

From SNPedia
Orientationplus
Stabilizedplus
Make rs6960920(C;C)
Make rs6960920(C;G)
Make rs6960920(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44376473
is asnp
is mentioned by
dbSNPrs6960920
dbSNP (old)rs6960920
ClinGenrs6960920
ebirs6960920
HLIrs6960920
Exacrs6960920
Gnomadrs6960920
Varsomers6960920
Maprs6960920
PheGenIrs6960920
Biobankrs6960920
1000 genomesrs6960920
hgdprs6960920
ensemblrs6960920
gopubmedrs6960920
geneviewrs6960920
scholarrs6960920
googlers6960920
pharmgkbrs6960920
gwascentralrs6960920
openSNPrs6960920
23andMers6960920
23andMe allrs6960920
SNPshotrs6960920
SNPdbers6960920
MSV3drs6960920
GWAS Ctlgrs6960920
GMAF0.4252
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 19727120OA-icon.png] Fine-Mapping of Vitiligo Susceptibility Loci on Chromosomes 7 and 9 and Interactions with NLRP1 (NALP1)