rs193922166

Orientation

plus

Stabilized

plus

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

Make rs193922166(-;-)

Make rs193922166(-;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

94427006

Gene

COL1A2

is a	snp
is	mentioned by
dbSNP	rs193922166
dbSNP (classic)	rs193922166
ClinGen	rs193922166
ebi	rs193922166
HLI	rs193922166
Exac	rs193922166
Gnomad	rs193922166
Varsome	rs193922166
LitVar	rs193922166
Map	rs193922166
PheGenI	rs193922166
Biobank	rs193922166
1000 genomes	rs193922166
hgdp	rs193922166
ensembl	rs193922166
geneview	rs193922166
scholar	rs193922166
google	rs193922166
pharmgkb	rs193922166
gwascentral	rs193922166
openSNP	rs193922166
23andMe	rs193922166
SNPshot	rs193922166
SNPdbe	rs193922166
MSV3d	rs193922166
GWAS Ctlg	rs193922166

Max Magnitude

0

ClinVar
Risk	rs193922166(-;-)
Alt	rs193922166(-;-)
Reference	Rs193922166(A;A)
Significance	Probable-Pathogenic
Disease	Osteogenesis imperfecta
Variation	info
Gene	COL1A2
CLNDBN	Osteogenesis imperfecta
Reversed	0
HGVS	NC_000007.13:g.94056318delA
CLNSRC	ClinVar
CLNACC	RCV000029602.1,