rs786205578

Orientation

minus

Stabilized

minus

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

Make rs786205578(A;A)

Make rs786205578(A;T)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

33186771

Gene

COL11A2

is a	snp
is	mentioned by
dbSNP	rs786205578
dbSNP (classic)	rs786205578
ClinGen	rs786205578
ebi	rs786205578
HLI	rs786205578
Exac	rs786205578
Gnomad	rs786205578
Varsome	rs786205578
LitVar	rs786205578
Map	rs786205578
PheGenI	rs786205578
Biobank	rs786205578
1000 genomes	rs786205578
hgdp	rs786205578
ensembl	rs786205578
geneview	rs786205578
scholar	rs786205578
google	rs786205578
pharmgkb	rs786205578
gwascentral	rs786205578
openSNP	rs786205578
23andMe	rs786205578
SNPshot	rs786205578
SNPdbe	rs786205578
MSV3d	rs786205578
GWAS Ctlg	rs786205578

Max Magnitude

0

ClinVar
Risk	rs786205578(A;A) rs786205578(C;C)
Alt	rs786205578(A;A) rs786205578(C;C)
Reference	Rs786205578(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	COL11A2
CLNDBN	not provided
Reversed	1
HGVS	NC_000006.11:g.33154548A>T
CLNSRC
CLNACC	RCV000171393.1,