rs61688134

Orientation

plus

Stabilized

plus

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

Make rs61688134(C;T)

Make rs61688134(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

21864476

Gene

ABCC9

is a	snp
is	mentioned by
dbSNP	rs61688134
dbSNP (classic)	rs61688134
ClinGen	rs61688134
ebi	rs61688134
HLI	rs61688134
Exac	rs61688134
Gnomad	rs61688134
Varsome	rs61688134
LitVar	rs61688134
Map	rs61688134
PheGenI	rs61688134
Biobank	rs61688134
1000 genomes	rs61688134
hgdp	rs61688134
ensembl	rs61688134
geneview	rs61688134
scholar	rs61688134
google	rs61688134
pharmgkb	rs61688134
gwascentral	rs61688134
openSNP	rs61688134
23andMe	rs61688134
SNPshot	rs61688134
SNPdbe	rs61688134
MSV3d	rs61688134
GWAS Ctlg	rs61688134

GMAF

0.00551

Max Magnitude

0

ClinVar
Risk	rs61688134(T;T)
Alt	rs61688134(T;T)
Reference	Rs61688134(C;C)
Significance	Probable-non-pathogenic
Disease	Cardiomyopathy not specified Myocardial infarction Dilated cardiomyopathy 1O Cardiovascular phenotype
Variation	info
Gene	ABCC9
CLNDBN	Cardiomyopathy not specified Myocardial infarction Dilated cardiomyopathy 1O Cardiovascular phenotype
Reversed	0
HGVS	NC_000012.11:g.22017410C>T
CLNSRC	ClinVar GeneDx LabCorp
CLNACC	RCV000029274.1, RCV000038600.4, RCV000172738.2, RCV000205535.2, RCV000251925.1,