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rs10768122

From SNPedia

Orientationplus
Stabilizedplus
Make rs10768122(A;A)
Make rs10768122(A;G)
Make rs10768122(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position35259305
GeneSLC1A2
is asnp
is mentioned by
dbSNPrs10768122
ebirs10768122
HLIrs10768122
Exacrs10768122
Varsomers10768122
Maprs10768122
PheGenIrs10768122
hapmaprs10768122
1000 genomesrs10768122
hgdprs10768122
ensemblrs10768122
gopubmedrs10768122
geneviewrs10768122
scholarrs10768122
googlers10768122
pharmgkbrs10768122
gwascentralrs10768122
openSNPrs10768122
23andMers10768122
23andMe allrs10768122
SNP Nexus

SNPshotrs10768122
SNPdbers10768122
MSV3drs10768122
GWAS Ctlgrs10768122
GMAF0.3439
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22561518OA-icon.png]
Trait
Title Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.
Risk Allele G
P-val 2E-9
Odds Ratio 1.2200 None