rs796052869

Orientation

plus

Stabilized

plus

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

Make rs796052869(A;T)

Make rs796052869(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

47946321

Gene

PNPO

is a	snp
is	mentioned by
dbSNP	rs796052869
dbSNP (classic)	rs796052869
ClinGen	rs796052869
ebi	rs796052869
HLI	rs796052869
Exac	rs796052869
Gnomad	rs796052869
Varsome	rs796052869
LitVar	rs796052869
Map	rs796052869
PheGenI	rs796052869
Biobank	rs796052869
1000 genomes	rs796052869
hgdp	rs796052869
ensembl	rs796052869
geneview	rs796052869
scholar	rs796052869
google	rs796052869
pharmgkb	rs796052869
gwascentral	rs796052869
openSNP	rs796052869
23andMe	rs796052869
SNPshot	rs796052869
SNPdbe	rs796052869
MSV3d	rs796052869
GWAS Ctlg	rs796052869

Max Magnitude

0

ClinVar
Risk	rs796052869(T;T)
Alt	rs796052869(T;T)
Reference	Rs796052869(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PNPO
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.46023687A>T
CLNSRC
CLNACC	RCV000188497.1,