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rs104894644

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894644(A;A)
Make rs104894644(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43755612
GeneSOST
is asnp
is mentioned by
dbSNPrs104894644
ebirs104894644
HLIrs104894644
Exacrs104894644
Varsomers104894644
Maprs104894644
PheGenIrs104894644
hapmaprs104894644
1000 genomesrs104894644
hgdprs104894644
ensemblrs104894644
gopubmedrs104894644
geneviewrs104894644
scholarrs104894644
googlers104894644
pharmgkbrs104894644
gwascentralrs104894644
openSNPrs104894644
23andMers104894644
23andMe allrs104894644
SNP Nexus

SNPshotrs104894644
SNPdbers104894644
MSV3drs104894644
GWAS Ctlgrs104894644
Max Magnitude0
OMIM605740
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894644(A;A)
Alt rs104894644(A;A)
Reference rs104894644(G;G)
Significance Pathogenic
Disease Sclerosteosis
Variation info
Gene SOST
CLNDBN Sclerosteosis
Reversed 1
HGVS NC_000017.10:g.41832980C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005051.3,