rs373890183

Orientation

plus

Stabilized

plus

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

Make rs373890183(A;A)

Make rs373890183(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

21848201

Gene

ABCC9

is a	snp
is	mentioned by
dbSNP	rs373890183
dbSNP (classic)	rs373890183
ClinGen	rs373890183
ebi	rs373890183
HLI	rs373890183
Exac	rs373890183
Gnomad	rs373890183
Varsome	rs373890183
LitVar	rs373890183
Map	rs373890183
PheGenI	rs373890183
Biobank	rs373890183
1000 genomes	rs373890183
hgdp	rs373890183
ensembl	rs373890183
geneview	rs373890183
scholar	rs373890183
google	rs373890183
pharmgkb	rs373890183
gwascentral	rs373890183
openSNP	rs373890183
23andMe	rs373890183
SNPshot	rs373890183
SNPdbe	rs373890183
MSV3d	rs373890183
GWAS Ctlg	rs373890183

Max Magnitude

0

ClinVar
Risk	rs373890183(A;A)
Alt	rs373890183(A;A)
Reference	Rs373890183(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ABCC9
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.22001135G>A
CLNSRC
CLNACC	RCV000171208.1,