rs121918620

Orientation

plus

Stabilized

plus

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

Make rs121918620(C;T)

Make rs121918620(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160128761

Gene

ATP1A2

is a	snp
is	mentioned by
dbSNP	rs121918620
dbSNP (classic)	rs121918620
ClinGen	rs121918620
ebi	rs121918620
HLI	rs121918620
Exac	rs121918620
Gnomad	rs121918620
Varsome	rs121918620
LitVar	rs121918620
Map	rs121918620
PheGenI	rs121918620
Biobank	rs121918620
1000 genomes	rs121918620
hgdp	rs121918620
ensembl	rs121918620
geneview	rs121918620
scholar	rs121918620
google	rs121918620
pharmgkb	rs121918620
gwascentral	rs121918620
openSNP	rs121918620
23andMe	rs121918620
SNPshot	rs121918620
SNPdbe	rs121918620
MSV3d	rs121918620
GWAS Ctlg	rs121918620

Max Magnitude

0

OMIM	182340
Desc
Variant	0014
Related	also

ClinVar
Risk	rs121918620(G;G) rs121918620(T;T)
Alt	rs121918620(G;G) rs121918620(T;T)
Reference	Rs121918620(C;C)
Significance	Pathogenic
Disease	not provided Familial hemiplegic migraine type 2
Variation	info
Gene	ATP1A2
CLNDBN	not provided Familial hemiplegic migraine type 2
Reversed	0
HGVS	NC_000001.10:g.160098551C>G; NC_000001.10:g.160098551C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000186787.1, RCV000013793.25,