rs137852960

Orientation

plus

Stabilized

plus

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

Make rs137852960(C;G)

Make rs137852960(G;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

3889670

Gene	LOC107985395, PANK2

is a	snp
is	mentioned by
dbSNP	rs137852960
dbSNP (classic)	rs137852960
ClinGen	rs137852960
ebi	rs137852960
HLI	rs137852960
Exac	rs137852960
Gnomad	rs137852960
Varsome	rs137852960
LitVar	rs137852960
Map	rs137852960
PheGenI	rs137852960
Biobank	rs137852960
1000 genomes	rs137852960
hgdp	rs137852960
ensembl	rs137852960
geneview	rs137852960
scholar	rs137852960
google	rs137852960
pharmgkb	rs137852960
gwascentral	rs137852960
openSNP	rs137852960
23andMe	rs137852960
SNPshot	rs137852960
SNPdbe	rs137852960
MSV3d	rs137852960
GWAS Ctlg	rs137852960

Max Magnitude

0

OMIM	606157
Desc
Variant	0003
Related	also

ClinVar
Risk	rs137852960(G;G)
Alt	rs137852960(G;G)
Reference	Rs137852960(C;C)
Significance	Pathogenic
Disease	Pigmentary pallidal degeneration
Variation	info
Gene	PANK2
CLNDBN	Pigmentary pallidal degeneration
Reversed	0
HGVS	NC_000020.10:g.3870317C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004809.3,