rs794729116

Orientation

minus

Stabilized

minus

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

Make rs794729116(A;A)

Make rs794729116(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

32802402

Gene

PKP2

is a	snp
is	mentioned by
dbSNP	rs794729116
dbSNP (classic)	rs794729116
ClinGen	rs794729116
ebi	rs794729116
HLI	rs794729116
Exac	rs794729116
Gnomad	rs794729116
Varsome	rs794729116
LitVar	rs794729116
Map	rs794729116
PheGenI	rs794729116
Biobank	rs794729116
1000 genomes	rs794729116
hgdp	rs794729116
ensembl	rs794729116
geneview	rs794729116
scholar	rs794729116
google	rs794729116
pharmgkb	rs794729116
gwascentral	rs794729116
openSNP	rs794729116
23andMe	rs794729116
SNPshot	rs794729116
SNPdbe	rs794729116
MSV3d	rs794729116
GWAS Ctlg	rs794729116

Max Magnitude

0

ClinVar
Risk	rs794729116(A;A) rs794729116(T;T)
Alt	rs794729116(A;A) rs794729116(T;T)
Reference	Rs794729116(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PKP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.32955336C>T
CLNSRC
CLNACC	RCV000183774.2,