rs387906805

Orientation

minus

Stabilized

minus

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

Make rs387906805(C;T)

Make rs387906805(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

21805184

Gene	ABCC9, LOC105369689

is a	snp
is	mentioned by
dbSNP	rs387906805
dbSNP (classic)	rs387906805
ClinGen	rs387906805
ebi	rs387906805
HLI	rs387906805
Exac	rs387906805
Gnomad	rs387906805
Varsome	rs387906805
LitVar	rs387906805
Map	rs387906805
PheGenI	rs387906805
Biobank	rs387906805
1000 genomes	rs387906805
hgdp	rs387906805
ensembl	rs387906805
geneview	rs387906805
scholar	rs387906805
google	rs387906805
pharmgkb	rs387906805
gwascentral	rs387906805
openSNP	rs387906805
23andMe	rs387906805
SNPshot	rs387906805
SNPdbe	rs387906805
MSV3d	rs387906805
GWAS Ctlg	rs387906805

Max Magnitude

0

ClinVar
Risk	rs387906805(T;T)
Alt	rs387906805(T;T)
Reference	Rs387906805(C;C)
Significance	Pathogenic
Disease	Atrial fibrillation
Variation	info
Gene	ABCC9
CLNDBN	Atrial fibrillation, familial, 12
Reversed	1
HGVS	NC_000012.11:g.21958118G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000023103.3,