rs794729099

Orientation

minus

Stabilized

minus

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

Make rs794729099(C;T)

Make rs794729099(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

32792699

Gene

PKP2

is a	snp
is	mentioned by
dbSNP	rs794729099
dbSNP (classic)	rs794729099
ClinGen	rs794729099
ebi	rs794729099
HLI	rs794729099
Exac	rs794729099
Gnomad	rs794729099
Varsome	rs794729099
LitVar	rs794729099
Map	rs794729099
PheGenI	rs794729099
Biobank	rs794729099
1000 genomes	rs794729099
hgdp	rs794729099
ensembl	rs794729099
geneview	rs794729099
scholar	rs794729099
google	rs794729099
pharmgkb	rs794729099
gwascentral	rs794729099
openSNP	rs794729099
23andMe	rs794729099
SNPshot	rs794729099
SNPdbe	rs794729099
MSV3d	rs794729099
GWAS Ctlg	rs794729099

Max Magnitude

0

ClinVar
Risk	rs794729099(T;T)
Alt	rs794729099(T;T)
Reference	Rs794729099(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PKP2
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.32945633G>A
CLNSRC
CLNACC	RCV000183717.2,