rs606231435

Orientation

minus

Stabilized

minus

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

Make rs606231435(A;A)

Make rs606231435(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

41970539

Gene

ATP1A3

is a	snp
is	mentioned by
dbSNP	rs606231435
dbSNP (classic)	rs606231435
ClinGen	rs606231435
ebi	rs606231435
HLI	rs606231435
Exac	rs606231435
Gnomad	rs606231435
Varsome	rs606231435
LitVar	rs606231435
Map	rs606231435
PheGenI	rs606231435
Biobank	rs606231435
1000 genomes	rs606231435
hgdp	rs606231435
ensembl	rs606231435
geneview	rs606231435
scholar	rs606231435
google	rs606231435
pharmgkb	rs606231435
gwascentral	rs606231435
openSNP	rs606231435
23andMe	rs606231435
SNPshot	rs606231435
SNPdbe	rs606231435
MSV3d	rs606231435
GWAS Ctlg	rs606231435

Max Magnitude

0

ClinVar
Risk	rs606231435(A;A)
Alt	rs606231435(A;A)
Reference	Rs606231435(G;G)
Significance	Pathogenic
Disease	Dystonia 12 not provided
Variation	info
Gene	ATP1A3
CLNDBN	Dystonia 12 not provided
Reversed	1
HGVS	NC_000019.9:g.42474691C>T
CLNSRC
CLNACC	RCV000148315.1, RCV000489717.1,