rs121918612

Orientation

plus

Stabilized

plus

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

Make rs121918612(A;A)

Make rs121918612(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160127704

Gene

ATP1A2

is a	snp
is	mentioned by
dbSNP	rs121918612
dbSNP (classic)	rs121918612
ClinGen	rs121918612
ebi	rs121918612
HLI	rs121918612
Exac	rs121918612
Gnomad	rs121918612
Varsome	rs121918612
LitVar	rs121918612
Map	rs121918612
PheGenI	rs121918612
Biobank	rs121918612
1000 genomes	rs121918612
hgdp	rs121918612
ensembl	rs121918612
geneview	rs121918612
scholar	rs121918612
google	rs121918612
pharmgkb	rs121918612
gwascentral	rs121918612
openSNP	rs121918612
23andMe	rs121918612
SNPshot	rs121918612
SNPdbe	rs121918612
MSV3d	rs121918612
GWAS Ctlg	rs121918612

Max Magnitude

0

OMIM	182340
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121918612(A;A)
Alt	rs121918612(A;A)
Reference	Rs121918612(G;G)
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.160097494G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013785.25,