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rs387906320

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906320(C;T)
Make rs387906320(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43758672
GeneSOST
is asnp
is mentioned by
dbSNPrs387906320
ebirs387906320
HLIrs387906320
Exacrs387906320
Varsomers387906320
Maprs387906320
PheGenIrs387906320
hapmaprs387906320
1000 genomesrs387906320
hgdprs387906320
ensemblrs387906320
gopubmedrs387906320
geneviewrs387906320
scholarrs387906320
googlers387906320
pharmgkbrs387906320
gwascentralrs387906320
openSNPrs387906320
23andMers387906320
23andMe allrs387906320
SNP Nexus

SNPshotrs387906320
SNPdbers387906320
MSV3drs387906320
GWAS Ctlgrs387906320
Max Magnitude0
ClinVar
Risk rs387906320(T;T)
Alt rs387906320(T;T)
Reference rs387906320(C;C)
Significance Pathogenic
Disease Sclerosteosis
Variation info
Gene SOST
CLNDBN Sclerosteosis
Reversed 1
HGVS NC_000017.10:g.41836040G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005049.3,