rs137852963

Orientation

plus

Stabilized

plus

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

Make rs137852963(A;A)

Make rs137852963(A;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

3912634

Gene

PANK2

is a	snp
is	mentioned by
dbSNP	rs137852963
dbSNP (classic)	rs137852963
ClinGen	rs137852963
ebi	rs137852963
HLI	rs137852963
Exac	rs137852963
Gnomad	rs137852963
Varsome	rs137852963
LitVar	rs137852963
Map	rs137852963
PheGenI	rs137852963
Biobank	rs137852963
1000 genomes	rs137852963
hgdp	rs137852963
ensembl	rs137852963
geneview	rs137852963
scholar	rs137852963
google	rs137852963
pharmgkb	rs137852963
gwascentral	rs137852963
openSNP	rs137852963
23andMe	rs137852963
SNPshot	rs137852963
SNPdbe	rs137852963
MSV3d	rs137852963
GWAS Ctlg	rs137852963

Max Magnitude

0

OMIM	606157
Desc
Variant	0006
Related	also

ClinVar
Risk	rs137852963(A;A)
Alt	rs137852963(A;A)
Reference	Rs137852963(G;G)
Significance	Pathogenic
Disease	Pigmentary pallidal degeneration
Variation	info
Gene	PANK2
CLNDBN	Pigmentary pallidal degeneration
Reversed	0
HGVS	NC_000020.10:g.3893281G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004812.2,