rs193922165

Orientation

plus

Stabilized

plus

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

Make rs193922165(A;A)

Make rs193922165(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

94425655

Gene

COL1A2

is a	snp
is	mentioned by
dbSNP	rs193922165
dbSNP (classic)	rs193922165
ClinGen	rs193922165
ebi	rs193922165
HLI	rs193922165
Exac	rs193922165
Gnomad	rs193922165
Varsome	rs193922165
LitVar	rs193922165
Map	rs193922165
PheGenI	rs193922165
Biobank	rs193922165
1000 genomes	rs193922165
hgdp	rs193922165
ensembl	rs193922165
geneview	rs193922165
scholar	rs193922165
google	rs193922165
pharmgkb	rs193922165
gwascentral	rs193922165
openSNP	rs193922165
23andMe	rs193922165
SNPshot	rs193922165
SNPdbe	rs193922165
MSV3d	rs193922165
GWAS Ctlg	rs193922165

Max Magnitude

0

ClinVar
Risk	rs193922165(A;A)
Alt	rs193922165(A;A)
Reference	Rs193922165(G;G)
Significance	Probable-Pathogenic
Disease	Osteogenesis imperfecta
Variation	info
Gene	COL1A2
CLNDBN	Osteogenesis imperfecta
Reversed	0
HGVS	NC_000007.13:g.94054967G>A
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029600.1,