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rs7758128

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs7758128(A;A)
Make rs7758128(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position32377506
GeneLOC101929163
is asnp
is mentioned by
dbSNPrs7758128
dbSNP (classic)rs7758128
ClinGenrs7758128
ebirs7758128
HLIrs7758128
Exacrs7758128
Gnomadrs7758128
Varsomers7758128
LitVarrs7758128
Maprs7758128
PheGenIrs7758128
Biobankrs7758128
1000 genomesrs7758128
hgdprs7758128
ensemblrs7758128
geneviewrs7758128
scholarrs7758128
googlers7758128
pharmgkbrs7758128
gwascentralrs7758128
openSNPrs7758128
23andMers7758128
SNPshotrs7758128
SNPdbers7758128
MSV3drs7758128
GWAS Ctlgrs7758128
GMAF0.04454
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS snp
PMID [PMID 21326295OA-icon.png]
Trait
Title Genome-Wide Analysis Identifies a Quantitative Trait Locus in the MHC Class II Region Associated with Generalized Vitiligo Age of Onset
Risk Allele A
P-val 8E-11
Odds Ratio None None
OMIM193200
Desc
Variant
Relatedalso