rs769266169

Orientation

plus

Stabilized

plus

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

Make rs769266169(C;T)

Make rs769266169(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

47946669

Gene

PNPO

is a	snp
is	mentioned by
dbSNP	rs769266169
dbSNP (classic)	rs769266169
ClinGen	rs769266169
ebi	rs769266169
HLI	rs769266169
Exac	rs769266169
Gnomad	rs769266169
Varsome	rs769266169
LitVar	rs769266169
Map	rs769266169
PheGenI	rs769266169
Biobank	rs769266169
1000 genomes	rs769266169
hgdp	rs769266169
ensembl	rs769266169
geneview	rs769266169
scholar	rs769266169
google	rs769266169
pharmgkb	rs769266169
gwascentral	rs769266169
openSNP	rs769266169
23andMe	rs769266169
SNPshot	rs769266169
SNPdbe	rs769266169
MSV3d	rs769266169
GWAS Ctlg	rs769266169

Max Magnitude

0

ClinVar
Risk	rs769266169(T;T)
Alt	rs769266169(T;T)
Reference	Rs769266169(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PNPO
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.46024035C>T
CLNSRC
CLNACC	RCV000188498.2,