rs766311956

Orientation

plus

Stabilized

plus

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

Make rs766311956(A;A)

Make rs766311956(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

47945594

Gene

PNPO

is a	snp
is	mentioned by
dbSNP	rs766311956
dbSNP (classic)	rs766311956
ClinGen	rs766311956
ebi	rs766311956
HLI	rs766311956
Exac	rs766311956
Gnomad	rs766311956
Varsome	rs766311956
LitVar	rs766311956
Map	rs766311956
PheGenI	rs766311956
Biobank	rs766311956
1000 genomes	rs766311956
hgdp	rs766311956
ensembl	rs766311956
geneview	rs766311956
scholar	rs766311956
google	rs766311956
pharmgkb	rs766311956
gwascentral	rs766311956
openSNP	rs766311956
23andMe	rs766311956
SNPshot	rs766311956
SNPdbe	rs766311956
MSV3d	rs766311956
GWAS Ctlg	rs766311956

Max Magnitude

0

ClinVar
Risk	rs766311956(A;A)
Alt	rs766311956(A;A)
Reference	Rs766311956(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PNPO
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.46022960G>A
CLNSRC
CLNACC	RCV000439228.1,