rs786205475

Orientation

minus

Stabilized

minus

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

Make rs786205475(C;T)

Make rs786205475(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

21838124

Gene

ABCC9

is a	snp
is	mentioned by
dbSNP	rs786205475
dbSNP (classic)	rs786205475
ClinGen	rs786205475
ebi	rs786205475
HLI	rs786205475
Exac	rs786205475
Gnomad	rs786205475
Varsome	rs786205475
LitVar	rs786205475
Map	rs786205475
PheGenI	rs786205475
Biobank	rs786205475
1000 genomes	rs786205475
hgdp	rs786205475
ensembl	rs786205475
geneview	rs786205475
scholar	rs786205475
google	rs786205475
pharmgkb	rs786205475
gwascentral	rs786205475
openSNP	rs786205475
23andMe	rs786205475
SNPshot	rs786205475
SNPdbe	rs786205475
MSV3d	rs786205475
GWAS Ctlg	rs786205475

Max Magnitude

0

ClinVar
Risk	rs786205475(T;T)
Alt	rs786205475(T;T)
Reference	Rs786205475(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ABCC9
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.21991058G>A
CLNSRC
CLNACC	RCV000171207.1,