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rs786200925

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786200925(C;C)
Make rs786200925(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position55479457
GeneWNT5A
is asnp
is mentioned by
dbSNPrs786200925
ebirs786200925
HLIrs786200925
Exacrs786200925
Varsomers786200925
Maprs786200925
PheGenIrs786200925
hapmaprs786200925
1000 genomesrs786200925
hgdprs786200925
ensemblrs786200925
gopubmedrs786200925
geneviewrs786200925
scholarrs786200925
googlers786200925
pharmgkbrs786200925
gwascentralrs786200925
openSNPrs786200925
23andMers786200925
23andMe allrs786200925
SNP Nexus

SNPshotrs786200925
SNPdbers786200925
MSV3drs786200925
GWAS Ctlgrs786200925
Max Magnitude0
ClinVar
Risk rs786200925(C;C)
Alt rs786200925(C;C)
Reference rs786200925(G;G)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene WNT5A
CLNDBN Robinow syndrome
Reversed 1
HGVS NC_000003.11:g.55513485C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000022696.28,