rs121918614

Orientation

plus

Stabilized

plus

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

Make rs121918614(A;A)

Make rs121918614(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160135470

Gene

ATP1A2

is a	snp
is	mentioned by
dbSNP	rs121918614
dbSNP (classic)	rs121918614
ClinGen	rs121918614
ebi	rs121918614
HLI	rs121918614
Exac	rs121918614
Gnomad	rs121918614
Varsome	rs121918614
LitVar	rs121918614
Map	rs121918614
PheGenI	rs121918614
Biobank	rs121918614
1000 genomes	rs121918614
hgdp	rs121918614
ensembl	rs121918614
geneview	rs121918614
scholar	rs121918614
google	rs121918614
pharmgkb	rs121918614
gwascentral	rs121918614
openSNP	rs121918614
23andMe	rs121918614
SNPshot	rs121918614
SNPdbe	rs121918614
MSV3d	rs121918614
GWAS Ctlg	rs121918614

Max Magnitude

0

OMIM	182340
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121918614(A;A)
Alt	rs121918614(A;A)
Reference	Rs121918614(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.160105260G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013787.25,