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rs9926296

From SNPedia

Orientationplus
Stabilizedplus
Make rs9926296(A;A)
Make rs9926296(A;G)
Make rs9926296(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position89751681
GeneFANCA
is asnp
is mentioned by
dbSNPrs9926296
dbSNP (old)rs9926296
ClinGenrs9926296
ebirs9926296
HLIrs9926296
Exacrs9926296
Gnomadrs9926296
Varsomers9926296
Maprs9926296
PheGenIrs9926296
Biobankrs9926296
1000 genomesrs9926296
hgdprs9926296
ensemblrs9926296
gopubmedrs9926296
geneviewrs9926296
scholarrs9926296
googlers9926296
pharmgkbrs9926296
gwascentralrs9926296
openSNPrs9926296
23andMers9926296
23andMe allrs9926296
SNP Nexus

SNPshotrs9926296
SNPdbers9926296
MSV3drs9926296
GWAS Ctlgrs9926296
GMAF0.3444
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 A
P-val 2E-13
Odds Ratio 1.2700 None