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rs59374417

From SNPedia

Orientationplus
Stabilizedplus
Make rs59374417(A;A)
Make rs59374417(A;C)
Make rs59374417(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position119569567
is asnp
is mentioned by
dbSNPrs59374417
ebirs59374417
HLIrs59374417
Exacrs59374417
Varsomers59374417
Maprs59374417
PheGenIrs59374417
hapmaprs59374417
1000 genomesrs59374417
hgdprs59374417
ensemblrs59374417
gopubmedrs59374417
geneviewrs59374417
scholarrs59374417
googlers59374417
pharmgkbrs59374417
gwascentralrs59374417
openSNPrs59374417
23andMers59374417
23andMe allrs59374417
SNP Nexus

SNPshotrs59374417
SNPdbers59374417
MSV3drs59374417
GWAS Ctlgrs59374417
GMAF0.1942
Max Magnitude
GWAS snp
PMID [PMID 22561518OA-icon.png]
Trait
Title Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.
Risk Allele C
P-val 4E-10
Odds Ratio 1.3400 None