rs767608725

Orientation

plus

Stabilized

plus

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

Make rs767608725(C;T)

Make rs767608725(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

55643177

Gene

PNPT1

is a	snp
is	mentioned by
dbSNP	rs767608725
dbSNP (classic)	rs767608725
ClinGen	rs767608725
ebi	rs767608725
HLI	rs767608725
Exac	rs767608725
Gnomad	rs767608725
Varsome	rs767608725
LitVar	rs767608725
Map	rs767608725
PheGenI	rs767608725
Biobank	rs767608725
1000 genomes	rs767608725
hgdp	rs767608725
ensembl	rs767608725
geneview	rs767608725
scholar	rs767608725
google	rs767608725
pharmgkb	rs767608725
gwascentral	rs767608725
openSNP	rs767608725
23andMe	rs767608725
SNPshot	rs767608725
SNPdbe	rs767608725
MSV3d	rs767608725
GWAS Ctlg	rs767608725

Max Magnitude

0

ClinVar
Risk	rs767608725(T;T)
Alt	rs767608725(T;T)
Reference	Rs767608725(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PNPT1
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.55870312C>T
CLNSRC
CLNACC	RCV000198071.1,