rs104894644

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs104894644(A;A)

Make rs104894644(A;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43755612

Gene

SOST

is a	snp
is	mentioned by
dbSNP	rs104894644
dbSNP (classic)	rs104894644
ClinGen	rs104894644
ebi	rs104894644
HLI	rs104894644
Exac	rs104894644
Gnomad	rs104894644
Varsome	rs104894644
LitVar	rs104894644
Map	rs104894644
PheGenI	rs104894644
Biobank	rs104894644
1000 genomes	rs104894644
hgdp	rs104894644
ensembl	rs104894644
geneview	rs104894644
scholar	rs104894644
google	rs104894644
pharmgkb	rs104894644
gwascentral	rs104894644
openSNP	rs104894644
23andMe	rs104894644
SNPshot	rs104894644
SNPdbe	rs104894644
MSV3d	rs104894644
GWAS Ctlg	rs104894644

Max Magnitude

0

OMIM	605740
Desc
Variant	0003
Related	also

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,