rs137852964

Orientation

plus

Stabilized

plus

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

Make rs137852964(C;C)

Make rs137852964(C;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

3910646

Gene

PANK2

is a	snp
is	mentioned by
dbSNP	rs137852964
dbSNP (classic)	rs137852964
ClinGen	rs137852964
ebi	rs137852964
HLI	rs137852964
Exac	rs137852964
Gnomad	rs137852964
Varsome	rs137852964
LitVar	rs137852964
Map	rs137852964
PheGenI	rs137852964
Biobank	rs137852964
1000 genomes	rs137852964
hgdp	rs137852964
ensembl	rs137852964
geneview	rs137852964
scholar	rs137852964
google	rs137852964
pharmgkb	rs137852964
gwascentral	rs137852964
openSNP	rs137852964
23andMe	rs137852964
SNPshot	rs137852964
SNPdbe	rs137852964
MSV3d	rs137852964
GWAS Ctlg	rs137852964

Max Magnitude

0

OMIM	606157
Desc
Variant	0007
Related	also

ClinVar
Risk	rs137852964(C;C)
Alt	rs137852964(C;C)
Reference	Rs137852964(T;T)
Significance	Pathogenic
Disease	Neurodegeneration with brain iron accumulation 1
Variation	info
Gene	PANK2
CLNDBN	Neurodegeneration with brain iron accumulation 1, atypical
Reversed	0
HGVS	NC_000020.10:g.3891293T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004813.2,