rs797044897

Orientation

minus

Stabilized

minus

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

Make rs797044897(A;G)

Make rs797044897(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

41984940

Gene

ATP1A3

is a	snp
is	mentioned by
dbSNP	rs797044897
dbSNP (classic)	rs797044897
ClinGen	rs797044897
ebi	rs797044897
HLI	rs797044897
Exac	rs797044897
Gnomad	rs797044897
Varsome	rs797044897
LitVar	rs797044897
Map	rs797044897
PheGenI	rs797044897
Biobank	rs797044897
1000 genomes	rs797044897
hgdp	rs797044897
ensembl	rs797044897
geneview	rs797044897
scholar	rs797044897
google	rs797044897
pharmgkb	rs797044897
gwascentral	rs797044897
openSNP	rs797044897
23andMe	rs797044897
SNPshot	rs797044897
SNPdbe	rs797044897
MSV3d	rs797044897
GWAS Ctlg	rs797044897

Max Magnitude

0

ClinVar
Risk	rs797044897(G;G)
Alt	rs797044897(G;G)
Reference	Rs797044897(A;A)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	ATP1A3
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000019.9:g.42489092T>C
CLNSRC
CLNACC	RCV000190721.1,