rs377328326

Orientation

plus

Stabilized

plus

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

Make rs377328326(A;A)

Make rs377328326(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

47945985

Gene

PNPO

is a	snp
is	mentioned by
dbSNP	rs377328326
dbSNP (classic)	rs377328326
ClinGen	rs377328326
ebi	rs377328326
HLI	rs377328326
Exac	rs377328326
Gnomad	rs377328326
Varsome	rs377328326
LitVar	rs377328326
Map	rs377328326
PheGenI	rs377328326
Biobank	rs377328326
1000 genomes	rs377328326
hgdp	rs377328326
ensembl	rs377328326
geneview	rs377328326
scholar	rs377328326
google	rs377328326
pharmgkb	rs377328326
gwascentral	rs377328326
openSNP	rs377328326
23andMe	rs377328326
SNPshot	rs377328326
SNPdbe	rs377328326
MSV3d	rs377328326
GWAS Ctlg	rs377328326

Max Magnitude

0

ClinVar
Risk	rs377328326(A;A) rs377328326(T;T)
Alt	rs377328326(A;A) rs377328326(T;T)
Reference	Rs377328326(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	PNPO
CLNDBN	not specified
Reversed	0
HGVS	NC_000017.10:g.46023351G>A
CLNSRC
CLNACC	RCV000188496.2,