rs146027425

Orientation

plus

Stabilized

plus

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

Make rs146027425(C;T)

Make rs146027425(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

47945924

Gene

PNPO

is a	snp
is	mentioned by
dbSNP	rs146027425
dbSNP (classic)	rs146027425
ClinGen	rs146027425
ebi	rs146027425
HLI	rs146027425
Exac	rs146027425
Gnomad	rs146027425
Varsome	rs146027425
LitVar	rs146027425
Map	rs146027425
PheGenI	rs146027425
Biobank	rs146027425
1000 genomes	rs146027425
hgdp	rs146027425
ensembl	rs146027425
geneview	rs146027425
scholar	rs146027425
google	rs146027425
pharmgkb	rs146027425
gwascentral	rs146027425
openSNP	rs146027425
23andMe	rs146027425
SNPshot	rs146027425
SNPdbe	rs146027425
MSV3d	rs146027425
GWAS Ctlg	rs146027425

Max Magnitude

0

ClinVar
Risk	rs146027425(G;G) rs146027425(T;T)
Alt	rs146027425(G;G) rs146027425(T;T)
Reference	Rs146027425(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PNPO
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.46023290C>T
CLNSRC
CLNACC	RCV000188494.2,