rs796052850

Orientation

minus

Stabilized

minus

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

Make rs796052850(C;T)

Make rs796052850(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

49864205

Gene

PNKP

is a	snp
is	mentioned by
dbSNP	rs796052850
dbSNP (classic)	rs796052850
ClinGen	rs796052850
ebi	rs796052850
HLI	rs796052850
Exac	rs796052850
Gnomad	rs796052850
Varsome	rs796052850
LitVar	rs796052850
Map	rs796052850
PheGenI	rs796052850
Biobank	rs796052850
1000 genomes	rs796052850
hgdp	rs796052850
ensembl	rs796052850
geneview	rs796052850
scholar	rs796052850
google	rs796052850
pharmgkb	rs796052850
gwascentral	rs796052850
openSNP	rs796052850
23andMe	rs796052850
SNPshot	rs796052850
SNPdbe	rs796052850
MSV3d	rs796052850
GWAS Ctlg	rs796052850

Max Magnitude

0

ClinVar
Risk	rs796052850(T;T)
Alt	rs796052850(T;T)
Reference	Rs796052850(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PNKP
CLNDBN	not provided
Reversed	1
HGVS	NC_000019.9:g.50367462G>A
CLNSRC
CLNACC	RCV000188430.1,