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rs869312850

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312850(C;C)
Make rs869312850(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position55474476
GeneWNT5A
is asnp
is mentioned by
dbSNPrs869312850
ebirs869312850
HLIrs869312850
Exacrs869312850
Varsomers869312850
Maprs869312850
PheGenIrs869312850
hapmaprs869312850
1000 genomesrs869312850
hgdprs869312850
ensemblrs869312850
gopubmedrs869312850
geneviewrs869312850
scholarrs869312850
googlers869312850
pharmgkbrs869312850
gwascentralrs869312850
openSNPrs869312850
23andMers869312850
23andMe allrs869312850
SNP Nexus

SNPshotrs869312850
SNPdbers869312850
MSV3drs869312850
GWAS Ctlgrs869312850
Max Magnitude0
ClinVar
Risk rs869312850(C;C)
Alt rs869312850(C;C)
Reference rs869312850(G;G)
Significance Pathogenic
Disease Robinow syndrome
Variation info
Gene WNT5A
CLNDBN Robinow syndrome
Reversed 1
HGVS NC_000003.11:g.55508504C>G
CLNSRC
CLNACC RCV000192022.1,