rs104894645

Orientation

minus

Stabilized

minus

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

Make rs104894645(C;T)

Make rs104894645(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43755608

Gene

SOST

is a	snp
is	mentioned by
dbSNP	rs104894645
dbSNP (classic)	rs104894645
ClinGen	rs104894645
ebi	rs104894645
HLI	rs104894645
Exac	rs104894645
Gnomad	rs104894645
Varsome	rs104894645
LitVar	rs104894645
Map	rs104894645
PheGenI	rs104894645
Biobank	rs104894645
1000 genomes	rs104894645
hgdp	rs104894645
ensembl	rs104894645
geneview	rs104894645
scholar	rs104894645
google	rs104894645
pharmgkb	rs104894645
gwascentral	rs104894645
openSNP	rs104894645
23andMe	rs104894645
SNPshot	rs104894645
SNPdbe	rs104894645
MSV3d	rs104894645
GWAS Ctlg	rs104894645

Max Magnitude

0

OMIM	605740
Desc
Variant	0004
Related	also

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,