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rs786205887

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205887(C;C)
Make rs786205887(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position46773719
GeneWNT3
is asnp
is mentioned by
dbSNPrs786205887
ebirs786205887
HLIrs786205887
Exacrs786205887
Varsomers786205887
Maprs786205887
PheGenIrs786205887
hapmaprs786205887
1000 genomesrs786205887
hgdprs786205887
ensemblrs786205887
gopubmedrs786205887
geneviewrs786205887
scholarrs786205887
googlers786205887
pharmgkbrs786205887
gwascentralrs786205887
openSNPrs786205887
23andMers786205887
23andMe allrs786205887
SNP Nexus

SNPshotrs786205887
SNPdbers786205887
MSV3drs786205887
GWAS Ctlgrs786205887
Max Magnitude0
ClinVar
Risk rs786205887(C;C)
Alt rs786205887(C;C)
Reference rs786205887(T;T)
Significance Probable-Pathogenic
Disease Exstrophy of the bladder
Variation info
Gene WNT3
CLNDBN Exstrophy of the bladder
Reversed 1
HGVS NC_000017.10:g.44851085A>G
CLNSRC
CLNACC RCV000172899.1,