rs193922168

Orientation

plus

Stabilized

plus

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

Make rs193922168(C;C)

Make rs193922168(C;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

94427714

Gene

COL1A2

is a	snp
is	mentioned by
dbSNP	rs193922168
dbSNP (classic)	rs193922168
ClinGen	rs193922168
ebi	rs193922168
HLI	rs193922168
Exac	rs193922168
Gnomad	rs193922168
Varsome	rs193922168
LitVar	rs193922168
Map	rs193922168
PheGenI	rs193922168
Biobank	rs193922168
1000 genomes	rs193922168
hgdp	rs193922168
ensembl	rs193922168
geneview	rs193922168
scholar	rs193922168
google	rs193922168
pharmgkb	rs193922168
gwascentral	rs193922168
openSNP	rs193922168
23andMe	rs193922168
SNPshot	rs193922168
SNPdbe	rs193922168
MSV3d	rs193922168
GWAS Ctlg	rs193922168

Max Magnitude

0

ClinVar
Risk	rs193922168(C;C)
Alt	rs193922168(C;C)
Reference	Rs193922168(G;G)
Significance	Probable-Pathogenic
Disease	Osteogenesis imperfecta
Variation	info
Gene	COL1A2
CLNDBN	Osteogenesis imperfecta
Reversed	0
HGVS	NC_000007.13:g.94057026G>C
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029605.1,