rs121908566

Orientation

plus

Stabilized

plus

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

Make rs121908566(C;T)

Make rs121908566(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

92040690

Gene

AKAP9

is a	snp
is	mentioned by
dbSNP	rs121908566
dbSNP (classic)	rs121908566
ClinGen	rs121908566
ebi	rs121908566
HLI	rs121908566
Exac	rs121908566
Gnomad	rs121908566
Varsome	rs121908566
LitVar	rs121908566
Map	rs121908566
PheGenI	rs121908566
Biobank	rs121908566
1000 genomes	rs121908566
hgdp	rs121908566
ensembl	rs121908566
geneview	rs121908566
scholar	rs121908566
google	rs121908566
pharmgkb	rs121908566
gwascentral	rs121908566
openSNP	rs121908566
23andMe	rs121908566
SNPshot	rs121908566
SNPdbe	rs121908566
MSV3d	rs121908566
GWAS Ctlg	rs121908566

Max Magnitude

0

OMIM	604001
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121908566(T;T)
Alt	rs121908566(T;T)
Reference	Rs121908566(C;C)
Significance	Pathogenic
Disease	Long QT syndrome 11
Variation	info
Gene	AKAP9
CLNDBN	Long QT syndrome 11
Reversed	0
HGVS	NC_000007.13:g.91670004C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006241.3,