rs1057517663

Orientation

minus

Stabilized

minus

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

Make rs1057517663(A;A)

Make rs1057517663(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

5

Position

151664183

Gene

SPARC

is a	snp
is	mentioned by
dbSNP	rs1057517663
dbSNP (classic)	rs1057517663
ClinGen	rs1057517663
ebi	rs1057517663
HLI	rs1057517663
Exac	rs1057517663
Gnomad	rs1057517663
Varsome	rs1057517663
LitVar	rs1057517663
Map	rs1057517663
PheGenI	rs1057517663
Biobank	rs1057517663
1000 genomes	rs1057517663
hgdp	rs1057517663
ensembl	rs1057517663
geneview	rs1057517663
scholar	rs1057517663
google	rs1057517663
pharmgkb	rs1057517663
gwascentral	rs1057517663
openSNP	rs1057517663
23andMe	rs1057517663
SNPshot	rs1057517663
SNPdbe	rs1057517663
MSV3d	rs1057517663
GWAS Ctlg	rs1057517663

Max Magnitude

0

ClinVar
Risk	rs1057517663(A;A)
Alt	rs1057517663(A;A)
Reference	Rs1057517663(G;G)
Significance	Pathogenic
Disease	Osteogenesis imperfecta
Variation	info
Gene	SPARC
CLNDBN	Osteogenesis imperfecta, type xvii
Reversed	1
HGVS	NC_000005.9:g.151043744C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000412523.1,