rs959497903

Orientation

plus

Stabilized

plus

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

Make rs959497903(C;T)

Make rs959497903(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

49862370

Gene

PNKP

is a	snp
is	mentioned by
dbSNP	rs959497903
dbSNP (classic)	rs959497903
ClinGen	rs959497903
ebi	rs959497903
HLI	rs959497903
Exac	rs959497903
Gnomad	rs959497903
Varsome	rs959497903
LitVar	rs959497903
Map	rs959497903
PheGenI	rs959497903
Biobank	rs959497903
1000 genomes	rs959497903
hgdp	rs959497903
ensembl	rs959497903
geneview	rs959497903
scholar	rs959497903
google	rs959497903
pharmgkb	rs959497903
gwascentral	rs959497903
openSNP	rs959497903
23andMe	rs959497903
SNPshot	rs959497903
SNPdbe	rs959497903
MSV3d	rs959497903
GWAS Ctlg	rs959497903

Max Magnitude

0

ClinVar
Risk	rs959497903(A;A) rs959497903(T;T)
Alt	rs959497903(A;A) rs959497903(T;T)
Reference	Rs959497903(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PNKP
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.50365627C>T
CLNSRC
CLNACC	RCV000489175.1,