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rs387907169

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907169(A;A)
Make rs387907169(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43758681
GeneSOST
is asnp
is mentioned by
dbSNPrs387907169
ebirs387907169
HLIrs387907169
Exacrs387907169
Varsomers387907169
Maprs387907169
PheGenIrs387907169
hapmaprs387907169
1000 genomesrs387907169
hgdprs387907169
ensemblrs387907169
gopubmedrs387907169
geneviewrs387907169
scholarrs387907169
googlers387907169
pharmgkbrs387907169
gwascentralrs387907169
openSNPrs387907169
23andMers387907169
23andMe allrs387907169
SNP Nexus

SNPshotrs387907169
SNPdbers387907169
MSV3drs387907169
GWAS Ctlgrs387907169
Max Magnitude0
ClinVar
Risk rs387907169(A;A)
Alt rs387907169(A;A)
Reference rs387907169(G;G)
Significance Pathogenic
Disease Craniodiaphyseal dysplasia
Variation info
Gene SOST
CLNDBN Craniodiaphyseal dysplasia, autosomal dominant
Reversed 1
HGVS NC_000017.10:g.41836049C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000024297.2,