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rs387906663

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906663(C;C)
Make rs387906663(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position55474477
GeneWNT5A
is asnp
is mentioned by
dbSNPrs387906663
ebirs387906663
HLIrs387906663
Exacrs387906663
Varsomers387906663
Maprs387906663
PheGenIrs387906663
hapmaprs387906663
1000 genomesrs387906663
hgdprs387906663
ensemblrs387906663
gopubmedrs387906663
geneviewrs387906663
scholarrs387906663
googlers387906663
pharmgkbrs387906663
gwascentralrs387906663
openSNPrs387906663
23andMers387906663
23andMe allrs387906663
SNP Nexus

SNPshotrs387906663
SNPdbers387906663
MSV3drs387906663
GWAS Ctlgrs387906663
Max Magnitude0
ClinVar
Risk rs387906663(C;C)
Alt rs387906663(C;C)
Reference rs387906663(T;T)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene WNT5A
CLNDBN Robinow syndrome
Reversed 1
HGVS NC_000003.11:g.55508505A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000022695.27,