rs794729100

Orientation

minus

Stabilized

minus

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

Make rs794729100(C;C)

Make rs794729100(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

32792690

Gene

PKP2

is a	snp
is	mentioned by
dbSNP	rs794729100
dbSNP (classic)	rs794729100
ClinGen	rs794729100
ebi	rs794729100
HLI	rs794729100
Exac	rs794729100
Gnomad	rs794729100
Varsome	rs794729100
LitVar	rs794729100
Map	rs794729100
PheGenI	rs794729100
Biobank	rs794729100
1000 genomes	rs794729100
hgdp	rs794729100
ensembl	rs794729100
geneview	rs794729100
scholar	rs794729100
google	rs794729100
pharmgkb	rs794729100
gwascentral	rs794729100
openSNP	rs794729100
23andMe	rs794729100
SNPshot	rs794729100
SNPdbe	rs794729100
MSV3d	rs794729100
GWAS Ctlg	rs794729100

Max Magnitude

0

ClinVar
Risk	rs794729100(C;C)
Alt	rs794729100(C;C)
Reference	Rs794729100(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PKP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.32945624A>G
CLNSRC
CLNACC	RCV000183718.1,