rs1057517662

Orientation

minus

Stabilized

minus

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

Make rs1057517662(A;A)

Make rs1057517662(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

5

Position

151667555

Gene

SPARC

is a	snp
is	mentioned by
dbSNP	rs1057517662
dbSNP (classic)	rs1057517662
ClinGen	rs1057517662
ebi	rs1057517662
HLI	rs1057517662
Exac	rs1057517662
Gnomad	rs1057517662
Varsome	rs1057517662
LitVar	rs1057517662
Map	rs1057517662
PheGenI	rs1057517662
Biobank	rs1057517662
1000 genomes	rs1057517662
hgdp	rs1057517662
ensembl	rs1057517662
geneview	rs1057517662
scholar	rs1057517662
google	rs1057517662
pharmgkb	rs1057517662
gwascentral	rs1057517662
openSNP	rs1057517662
23andMe	rs1057517662
SNPshot	rs1057517662
SNPdbe	rs1057517662
MSV3d	rs1057517662
GWAS Ctlg	rs1057517662

Max Magnitude

0

ClinVar
Risk	rs1057517662(A;A)
Alt	rs1057517662(A;A)
Reference	Rs1057517662(G;G)
Significance	Pathogenic
Disease	Osteogenesis imperfecta
Variation	info
Gene	SPARC
CLNDBN	Osteogenesis imperfecta, type xvii
Reversed	1
HGVS	NC_000005.9:g.151047116C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000412625.1,