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rs104894645

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894645(C;T)
Make rs104894645(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43755608
GeneSOST
is asnp
is mentioned by
dbSNPrs104894645
ebirs104894645
HLIrs104894645
Exacrs104894645
Varsomers104894645
Maprs104894645
PheGenIrs104894645
hapmaprs104894645
1000 genomesrs104894645
hgdprs104894645
ensemblrs104894645
gopubmedrs104894645
geneviewrs104894645
scholarrs104894645
googlers104894645
pharmgkbrs104894645
gwascentralrs104894645
openSNPrs104894645
23andMers104894645
23andMe allrs104894645
SNP Nexus

SNPshotrs104894645
SNPdbers104894645
MSV3drs104894645
GWAS Ctlgrs104894645
Max Magnitude0
OMIM605740
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104894645(T;T)
Alt rs104894645(T;T)
Reference rs104894645(C;C)
Significance Pathogenic
Disease Sclerosteosis
Variation info
Gene SOST
CLNDBN Sclerosteosis
Reversed 1
HGVS NC_000017.10:g.41832976G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005052.3,