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rs786204837

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204837(A;A)
Make rs786204837(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position55479499
GeneWNT5A
is asnp
is mentioned by
dbSNPrs786204837
ebirs786204837
HLIrs786204837
Exacrs786204837
Varsomers786204837
Maprs786204837
PheGenIrs786204837
hapmaprs786204837
1000 genomesrs786204837
hgdprs786204837
ensemblrs786204837
gopubmedrs786204837
geneviewrs786204837
scholarrs786204837
googlers786204837
pharmgkbrs786204837
gwascentralrs786204837
openSNPrs786204837
23andMers786204837
23andMe allrs786204837
SNP Nexus

SNPshotrs786204837
SNPdbers786204837
MSV3drs786204837
GWAS Ctlgrs786204837
Max Magnitude0
ClinVar
Risk rs786204837(A;A)
Alt rs786204837(A;A)
Reference rs786204837(G;G)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene WNT5A
CLNDBN Robinow syndrome
Reversed 1
HGVS NC_000003.11:g.55513527C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000169741.5,