rs796052861

Orientation

minus

Stabilized

minus

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

Make rs796052861(-;CGCCAGGT)

Make rs796052861(CGCCAGGT;CGCCAGGT)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

49861769

Gene

PNKP

is a	snp
is	mentioned by
dbSNP	rs796052861
dbSNP (classic)	rs796052861
ClinGen	rs796052861
ebi	rs796052861
HLI	rs796052861
Exac	rs796052861
Gnomad	rs796052861
Varsome	rs796052861
LitVar	rs796052861
Map	rs796052861
PheGenI	rs796052861
Biobank	rs796052861
1000 genomes	rs796052861
hgdp	rs796052861
ensembl	rs796052861
geneview	rs796052861
scholar	rs796052861
google	rs796052861
pharmgkb	rs796052861
gwascentral	rs796052861
openSNP	rs796052861
23andMe	rs796052861
SNPshot	rs796052861
SNPdbe	rs796052861
MSV3d	rs796052861
GWAS Ctlg	rs796052861

Max Magnitude

0

ClinVar
Risk	rs796052861(CGCCAGGT;CGCCAGGT)
Alt	rs796052861(CGCCAGGT;CGCCAGGT)
Reference	Rs796052861(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PNKP
CLNDBN	not provided
Reversed	1
HGVS	NC_000019.9:g.50365027_50365034dupACCTGGCG
CLNSRC
CLNACC	RCV000188472.1,