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rs786204836

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204836(A;G)
Make rs786204836(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position55479448
GeneWNT5A
is asnp
is mentioned by
dbSNPrs786204836
ebirs786204836
HLIrs786204836
Exacrs786204836
Varsomers786204836
Maprs786204836
PheGenIrs786204836
hapmaprs786204836
1000 genomesrs786204836
hgdprs786204836
ensemblrs786204836
gopubmedrs786204836
geneviewrs786204836
scholarrs786204836
googlers786204836
pharmgkbrs786204836
gwascentralrs786204836
openSNPrs786204836
23andMers786204836
23andMe allrs786204836
SNP Nexus

SNPshotrs786204836
SNPdbers786204836
MSV3drs786204836
GWAS Ctlgrs786204836
Max Magnitude0
ClinVar
Risk rs786204836(G;G)
Alt rs786204836(G;G)
Reference rs786204836(A;A)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene WNT5A
CLNDBN Robinow syndrome
Reversed 1
HGVS NC_000003.11:g.55513476T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000169740.5,