rs137852961

Orientation

plus

Stabilized

plus

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

Make rs137852961(C;T)

Make rs137852961(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

3908087

Gene

PANK2

is a	snp
is	mentioned by
dbSNP	rs137852961
dbSNP (classic)	rs137852961
ClinGen	rs137852961
ebi	rs137852961
HLI	rs137852961
Exac	rs137852961
Gnomad	rs137852961
Varsome	rs137852961
LitVar	rs137852961
Map	rs137852961
PheGenI	rs137852961
Biobank	rs137852961
1000 genomes	rs137852961
hgdp	rs137852961
ensembl	rs137852961
geneview	rs137852961
scholar	rs137852961
google	rs137852961
pharmgkb	rs137852961
gwascentral	rs137852961
openSNP	rs137852961
23andMe	rs137852961
SNPshot	rs137852961
SNPdbe	rs137852961
MSV3d	rs137852961
GWAS Ctlg	rs137852961

Max Magnitude

0

OMIM	606157
Desc
Variant	0004
Related	also

ClinVar
Risk	rs137852961(T;T)
Alt	rs137852961(T;T)
Reference	Rs137852961(C;C)
Significance	Pathogenic
Disease	Pigmentary pallidal degeneration
Variation	info
Gene	PANK2
CLNDBN	Pigmentary pallidal degeneration
Reversed	0
HGVS	NC_000020.10:g.3888734C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004810.2,