rs794728955

Orientation

minus

Stabilized

minus

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

Make rs794728955(A;T)

Make rs794728955(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

21845685

Gene

ABCC9

is a	snp
is	mentioned by
dbSNP	rs794728955
dbSNP (classic)	rs794728955
ClinGen	rs794728955
ebi	rs794728955
HLI	rs794728955
Exac	rs794728955
Gnomad	rs794728955
Varsome	rs794728955
LitVar	rs794728955
Map	rs794728955
PheGenI	rs794728955
Biobank	rs794728955
1000 genomes	rs794728955
hgdp	rs794728955
ensembl	rs794728955
geneview	rs794728955
scholar	rs794728955
google	rs794728955
pharmgkb	rs794728955
gwascentral	rs794728955
openSNP	rs794728955
23andMe	rs794728955
SNPshot	rs794728955
SNPdbe	rs794728955
MSV3d	rs794728955
GWAS Ctlg	rs794728955

Max Magnitude

0

ClinVar
Risk	rs794728955(T;T)
Alt	rs794728955(T;T)
Reference	Rs794728955(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ABCC9
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.21998619T>A
CLNSRC
CLNACC	RCV000183234.1,