rs753376100

Orientation

plus

Stabilized

plus

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

Make rs753376100(C;T)

Make rs753376100(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

3910664

Gene

PANK2

is a	snp
is	mentioned by
dbSNP	rs753376100
dbSNP (classic)	rs753376100
ClinGen	rs753376100
ebi	rs753376100
HLI	rs753376100
Exac	rs753376100
Gnomad	rs753376100
Varsome	rs753376100
LitVar	rs753376100
Map	rs753376100
PheGenI	rs753376100
Biobank	rs753376100
1000 genomes	rs753376100
hgdp	rs753376100
ensembl	rs753376100
geneview	rs753376100
scholar	rs753376100
google	rs753376100
pharmgkb	rs753376100
gwascentral	rs753376100
openSNP	rs753376100
23andMe	rs753376100
SNPshot	rs753376100
SNPdbe	rs753376100
MSV3d	rs753376100
GWAS Ctlg	rs753376100

Max Magnitude

0

ClinVar
Risk	rs753376100(T;T)
Alt	rs753376100(T;T)
Reference	Rs753376100(C;C)
Significance	Pathogenic
Disease	Neurodegeneration
Variation	info
Gene	PANK2
CLNDBN	Neurodegeneration
Reversed	0
HGVS	NC_000020.10:g.3891311C>T
CLNSRC
CLNACC	RCV000414787.1,