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rs121918261

From SNPedia

Orientationplus
Stabilizedplus
Make rs121918261(G;G)
Make rs121918261(G;T)
Make rs121918261(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position39339703
GeneLOC105375239, POU6F2
is asnp
is mentioned by
dbSNPrs121918261
dbSNP (old)rs121918261
ClinGenrs121918261
ebirs121918261
HLIrs121918261
Exacrs121918261
Gnomadrs121918261
Varsomers121918261
Maprs121918261
PheGenIrs121918261
Biobankrs121918261
1000 genomesrs121918261
hgdprs121918261
ensemblrs121918261
gopubmedrs121918261
geneviewrs121918261
scholarrs121918261
googlers121918261
pharmgkbrs121918261
gwascentralrs121918261
openSNPrs121918261
23andMers121918261
23andMe allrs121918261
SNP Nexus

SNPshotrs121918261
SNPdbers121918261
MSV3drs121918261
GWAS Ctlgrs121918261
Max Magnitude
OMIM609062
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918261(T;T)
Alt rs121918261(T;T)
Reference rs121918261(G;G)
Significance Other
Disease Wilms tumor and radial bilateral aplasia
Variation info
Gene POU6F2
CLNDBN Wilms tumor and radial bilateral aplasia
Reversed 0
HGVS NC_000007.13:g.39379302G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001948.2,