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rs776155094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs776155094(-;-)
Make rs776155094(-;C)
ReferenceGRCh38.p7 38.3/149
Chromosome11
Position32435210
GeneWT1, WT1-AS
is asnp
is mentioned by
dbSNPrs776155094
dbSNP (classic)rs776155094
ClinGenrs776155094
ebirs776155094
HLIrs776155094
Exacrs776155094
Gnomadrs776155094
Varsomers776155094
LitVarrs776155094
Maprs776155094
PheGenIrs776155094
Biobankrs776155094
1000 genomesrs776155094
hgdprs776155094
ensemblrs776155094
geneviewrs776155094
scholarrs776155094
googlers776155094
pharmgkbrs776155094
gwascentralrs776155094
openSNPrs776155094
23andMers776155094
23andMe allrs776155094
SNPshotrs776155094
SNPdbers776155094
MSV3drs776155094
GWAS Ctlgrs776155094
Max Magnitude0
ClinVar
Risk rs776155094(-;-)
Alt rs776155094(-;-)
Reference Rs776155094(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WT1 WT1-AS
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.32456756delC
CLNSRC
CLNACC RCV000255852.1,