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rs387907231

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907231(A;A)
Make rs387907231(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position13819384
GeneWNT7A
is asnp
is mentioned by
dbSNPrs387907231
ebirs387907231
HLIrs387907231
Exacrs387907231
Varsomers387907231
Maprs387907231
PheGenIrs387907231
hapmaprs387907231
1000 genomesrs387907231
hgdprs387907231
ensemblrs387907231
gopubmedrs387907231
geneviewrs387907231
scholarrs387907231
googlers387907231
pharmgkbrs387907231
gwascentralrs387907231
openSNPrs387907231
23andMers387907231
23andMe allrs387907231
SNP Nexus

SNPshotrs387907231
SNPdbers387907231
MSV3drs387907231
GWAS Ctlgrs387907231
Max Magnitude0
ClinVar
Risk rs387907231(A;A)
Alt rs387907231(A;A)
Reference rs387907231(G;G)
Significance Pathogenic
Disease Ulna and fibula absence of with severe limb deficiency
Variation info
Gene WNT7A
CLNDBN Ulna and fibula absence of with severe limb deficiency
Reversed 1
HGVS NC_000003.11:g.13860881C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000029192.2,