rs606231226

Orientation

plus

Stabilized

plus

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

Make rs606231226(C;T)

Make rs606231226(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

154305155

Gene

DPP6

is a	snp
is	mentioned by
dbSNP	rs606231226
dbSNP (classic)	rs606231226
ClinGen	rs606231226
ebi	rs606231226
HLI	rs606231226
Exac	rs606231226
Gnomad	rs606231226
Varsome	rs606231226
LitVar	rs606231226
Map	rs606231226
PheGenI	rs606231226
Biobank	rs606231226
1000 genomes	rs606231226
hgdp	rs606231226
ensembl	rs606231226
geneview	rs606231226
scholar	rs606231226
google	rs606231226
pharmgkb	rs606231226
gwascentral	rs606231226
openSNP	rs606231226
23andMe	rs606231226
SNPshot	rs606231226
SNPdbe	rs606231226
MSV3d	rs606231226
GWAS Ctlg	rs606231226

Max Magnitude

0

ClinVar
Risk	rs606231226(T;T)
Alt	rs606231226(T;T)
Reference	Rs606231226(C;C)
Significance	Pathogenic
Disease	Ventricular fibrillation
Variation	info
Gene	DPP6
CLNDBN	Ventricular fibrillation, paroxysmal familial, 2
Reversed	0
HGVS	NC_000007.14:g.154305155C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018285.28,