rs768569721

Orientation

plus

Stabilized

plus

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

Make rs768569721(A;A)

Make rs768569721(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

33176294

Gene

COL11A2

is a	snp
is	mentioned by
dbSNP	rs768569721
dbSNP (classic)	rs768569721
ClinGen	rs768569721
ebi	rs768569721
HLI	rs768569721
Exac	rs768569721
Gnomad	rs768569721
Varsome	rs768569721
LitVar	rs768569721
Map	rs768569721
PheGenI	rs768569721
Biobank	rs768569721
1000 genomes	rs768569721
hgdp	rs768569721
ensembl	rs768569721
geneview	rs768569721
scholar	rs768569721
google	rs768569721
pharmgkb	rs768569721
gwascentral	rs768569721
openSNP	rs768569721
23andMe	rs768569721
SNPshot	rs768569721
SNPdbe	rs768569721
MSV3d	rs768569721
GWAS Ctlg	rs768569721

Max Magnitude

0

ClinVar
Risk	rs768569721(A;A) rs768569721(T;T)
Alt	rs768569721(A;A) rs768569721(T;T)
Reference	Rs768569721(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	COL11A2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.33144071C>A
CLNSRC
CLNACC	RCV000425711.1,