rs67707918

Orientation

plus

Stabilized

plus

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

Make rs67707918(A;A)

Make rs67707918(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

94410501

Gene

COL1A2

is a	snp
is	mentioned by
dbSNP	rs67707918
dbSNP (classic)	rs67707918
ClinGen	rs67707918
ebi	rs67707918
HLI	rs67707918
Exac	rs67707918
Gnomad	rs67707918
Varsome	rs67707918
LitVar	rs67707918
Map	rs67707918
PheGenI	rs67707918
Biobank	rs67707918
1000 genomes	rs67707918
hgdp	rs67707918
ensembl	rs67707918
geneview	rs67707918
scholar	rs67707918
google	rs67707918
pharmgkb	rs67707918
gwascentral	rs67707918
openSNP	rs67707918
23andMe	rs67707918
SNPshot	rs67707918
SNPdbe	rs67707918
MSV3d	rs67707918
GWAS Ctlg	rs67707918

Max Magnitude

0

ClinVar
Risk	rs67707918(A;A) rs67707918(T;T)
Alt	rs67707918(A;A) rs67707918(T;T)
Reference	Rs67707918(G;G)
Significance	Pathogenic
Disease	Osteogenesis imperfecta with normal sclerae
Variation	info
Gene	COL1A2
CLNDBN	Osteogenesis imperfecta with normal sclerae, dominant form
Reversed	0
HGVS	NC_000007.13:g.94039813G>A
CLNSRC
CLNACC	RCV000490690.1,