rs797044915

Orientation

minus

Stabilized

minus

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

Make rs797044915(G;T)

Make rs797044915(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

33176015

Gene

COL11A2

is a	snp
is	mentioned by
dbSNP	rs797044915
dbSNP (classic)	rs797044915
ClinGen	rs797044915
ebi	rs797044915
HLI	rs797044915
Exac	rs797044915
Gnomad	rs797044915
Varsome	rs797044915
LitVar	rs797044915
Map	rs797044915
PheGenI	rs797044915
Biobank	rs797044915
1000 genomes	rs797044915
hgdp	rs797044915
ensembl	rs797044915
geneview	rs797044915
scholar	rs797044915
google	rs797044915
pharmgkb	rs797044915
gwascentral	rs797044915
openSNP	rs797044915
23andMe	rs797044915
SNPshot	rs797044915
SNPdbe	rs797044915
MSV3d	rs797044915
GWAS Ctlg	rs797044915

Max Magnitude

0

ClinVar
Risk	rs797044915(T;T)
Alt	rs797044915(T;T)
Reference	Rs797044915(G;G)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	COL11A2
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000006.11:g.33143792C>A
CLNSRC
CLNACC	RCV000190748.1,