rs121908990

Orientation

minus

Stabilized

minus

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

Make rs121908990(C;G)

Make rs121908990(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

151560611

Gene

PRKAG2

is a	snp
is	mentioned by
dbSNP	rs121908990
dbSNP (classic)	rs121908990
ClinGen	rs121908990
ebi	rs121908990
HLI	rs121908990
Exac	rs121908990
Gnomad	rs121908990
Varsome	rs121908990
LitVar	rs121908990
Map	rs121908990
PheGenI	rs121908990
Biobank	rs121908990
1000 genomes	rs121908990
hgdp	rs121908990
ensembl	rs121908990
geneview	rs121908990
scholar	rs121908990
google	rs121908990
pharmgkb	rs121908990
gwascentral	rs121908990
openSNP	rs121908990
23andMe	rs121908990
SNPshot	rs121908990
SNPdbe	rs121908990
MSV3d	rs121908990
GWAS Ctlg	rs121908990

Max Magnitude

0

OMIM	602743
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121908990(G;G) rs121908990(T;T)
Alt	rs121908990(G;G) rs121908990(T;T)
Reference	Rs121908990(C;C)
Significance	Pathogenic
Disease	Wolff-Parkinson-White syndrome
Variation	info
Gene	PRKAG2
CLNDBN	Wolff-Parkinson-White syndrome, childhood-onset
Reversed	1
HGVS	NC_000007.13:g.151257697G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007254.4,