rs794727669

Orientation

plus

Stabilized

plus

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

Make rs794727669(G;T)

Make rs794727669(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

94425136

Gene

COL1A2

is a	snp
is	mentioned by
dbSNP	rs794727669
dbSNP (classic)	rs794727669
ClinGen	rs794727669
ebi	rs794727669
HLI	rs794727669
Exac	rs794727669
Gnomad	rs794727669
Varsome	rs794727669
LitVar	rs794727669
Map	rs794727669
PheGenI	rs794727669
Biobank	rs794727669
1000 genomes	rs794727669
hgdp	rs794727669
ensembl	rs794727669
geneview	rs794727669
scholar	rs794727669
google	rs794727669
pharmgkb	rs794727669
gwascentral	rs794727669
openSNP	rs794727669
23andMe	rs794727669
SNPshot	rs794727669
SNPdbe	rs794727669
MSV3d	rs794727669
GWAS Ctlg	rs794727669

Max Magnitude

0

ClinVar
Risk	rs794727669(T;T)
Alt	rs794727669(T;T)
Reference	Rs794727669(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	COL1A2
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.94054448G>T
CLNSRC
CLNACC	RCV000178479.1,