rs137852965

Orientation

plus

Stabilized

plus

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

Make rs137852965(A;G)

Make rs137852965(G;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

3907997

Gene

PANK2

is a	snp
is	mentioned by
dbSNP	rs137852965
dbSNP (classic)	rs137852965
ClinGen	rs137852965
ebi	rs137852965
HLI	rs137852965
Exac	rs137852965
Gnomad	rs137852965
Varsome	rs137852965
LitVar	rs137852965
Map	rs137852965
PheGenI	rs137852965
Biobank	rs137852965
1000 genomes	rs137852965
hgdp	rs137852965
ensembl	rs137852965
geneview	rs137852965
scholar	rs137852965
google	rs137852965
pharmgkb	rs137852965
gwascentral	rs137852965
openSNP	rs137852965
23andMe	rs137852965
SNPshot	rs137852965
SNPdbe	rs137852965
MSV3d	rs137852965
GWAS Ctlg	rs137852965

Max Magnitude

0

OMIM	606157
Desc
Variant	0008
Related	also

ClinVar
Risk	rs137852965(G;G)
Alt	rs137852965(G;G)
Reference	Rs137852965(A;A)
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.3888644A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004814.2,