rs121918613

Orientation

plus

Stabilized

plus

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

Make rs121918613(A;G)

Make rs121918613(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160128667

Gene

ATP1A2

is a	snp
is	mentioned by
dbSNP	rs121918613
dbSNP (classic)	rs121918613
ClinGen	rs121918613
ebi	rs121918613
HLI	rs121918613
Exac	rs121918613
Gnomad	rs121918613
Varsome	rs121918613
LitVar	rs121918613
Map	rs121918613
PheGenI	rs121918613
Biobank	rs121918613
1000 genomes	rs121918613
hgdp	rs121918613
ensembl	rs121918613
geneview	rs121918613
scholar	rs121918613
google	rs121918613
pharmgkb	rs121918613
gwascentral	rs121918613
openSNP	rs121918613
23andMe	rs121918613
SNPshot	rs121918613
SNPdbe	rs121918613
MSV3d	rs121918613
GWAS Ctlg	rs121918613

Max Magnitude

0

OMIM	182340
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121918613(G;G)
Alt	rs121918613(G;G)
Reference	Rs121918613(A;A)
Significance	Pathogenic
Disease	Familial hemiplegic migraine type 2
Variation	info
Gene	ATP1A2
CLNDBN	Familial hemiplegic migraine type 2
Reversed	0
HGVS	NC_000001.10:g.160098457A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013786.24,