rs121918619

Orientation

plus

Stabilized

plus

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

Make rs121918619(C;T)

Make rs121918619(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160123228

Gene

ATP1A2

is a	snp
is	mentioned by
dbSNP	rs121918619
dbSNP (classic)	rs121918619
ClinGen	rs121918619
ebi	rs121918619
HLI	rs121918619
Exac	rs121918619
Gnomad	rs121918619
Varsome	rs121918619
LitVar	rs121918619
Map	rs121918619
PheGenI	rs121918619
Biobank	rs121918619
1000 genomes	rs121918619
hgdp	rs121918619
ensembl	rs121918619
geneview	rs121918619
scholar	rs121918619
google	rs121918619
pharmgkb	rs121918619
gwascentral	rs121918619
openSNP	rs121918619
23andMe	rs121918619
SNPshot	rs121918619
SNPdbe	rs121918619
MSV3d	rs121918619
GWAS Ctlg	rs121918619

Max Magnitude

0

OMIM	182340
Desc
Variant	0013
Related	also

ClinVar
Risk	rs121918619(T;T)
Alt	rs121918619(T;T)
Reference	Rs121918619(C;C)
Significance	Pathogenic
Disease	Familial hemiplegic migraine type 2 not specified
Variation	info
Gene	ATP1A2
CLNDBN	Familial hemiplegic migraine type 2 not specified
Reversed	0
HGVS	NC_000001.10:g.160093018C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013792.24, RCV000442150.1,