rs78897684

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;G)	6.7	Arrhythmogenic right ventricular dysplasia

Make rs78897684(A;A)

Make rs78897684(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

32824163

Gene

PKP2

is a	snp
is	mentioned by
dbSNP	rs78897684
dbSNP (classic)	rs78897684
ClinGen	rs78897684
ebi	rs78897684
HLI	rs78897684
Exac	rs78897684
Gnomad	rs78897684
Varsome	rs78897684
LitVar	rs78897684
Map	rs78897684
PheGenI	rs78897684
Biobank	rs78897684
1000 genomes	rs78897684
hgdp	rs78897684
ensembl	rs78897684
geneview	rs78897684
scholar	rs78897684
google	rs78897684
pharmgkb	rs78897684
gwascentral	rs78897684
openSNP	rs78897684
23andMe	rs78897684
SNPshot	rs78897684
SNPdbe	rs78897684
MSV3d	rs78897684
GWAS Ctlg	rs78897684

Max Magnitude

6.7

ClinVar
Risk	rs78897684(A;A) rs78897684(G;G)
Alt	rs78897684(A;A) rs78897684(G;G)
Reference	Rs78897684(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PKP2
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.32977097C>G
CLNSRC
CLNACC	RCV000183751.3,