rs121918617

Orientation

plus

Stabilized

plus

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

Make rs121918617(C;C)

Make rs121918617(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160127660

Gene

ATP1A2

is a	snp
is	mentioned by
dbSNP	rs121918617
dbSNP (classic)	rs121918617
ClinGen	rs121918617
ebi	rs121918617
HLI	rs121918617
Exac	rs121918617
Gnomad	rs121918617
Varsome	rs121918617
LitVar	rs121918617
Map	rs121918617
PheGenI	rs121918617
Biobank	rs121918617
1000 genomes	rs121918617
hgdp	rs121918617
ensembl	rs121918617
geneview	rs121918617
scholar	rs121918617
google	rs121918617
pharmgkb	rs121918617
gwascentral	rs121918617
openSNP	rs121918617
23andMe	rs121918617
SNPshot	rs121918617
SNPdbe	rs121918617
MSV3d	rs121918617
GWAS Ctlg	rs121918617

Max Magnitude

0

OMIM	182340
Desc
Variant	0011
Related	also

ClinVar
Risk	rs121918617(C;C)
Alt	rs121918617(C;C)
Reference	Rs121918617(T;T)
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.160097450T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013790.26,