rs121918618

Orientation

plus

Stabilized

plus

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

Make rs121918618(C;T)

Make rs121918618(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160129007

Gene

ATP1A2

is a	snp
is	mentioned by
dbSNP	rs121918618
dbSNP (classic)	rs121918618
ClinGen	rs121918618
ebi	rs121918618
HLI	rs121918618
Exac	rs121918618
Gnomad	rs121918618
Varsome	rs121918618
LitVar	rs121918618
Map	rs121918618
PheGenI	rs121918618
Biobank	rs121918618
1000 genomes	rs121918618
hgdp	rs121918618
ensembl	rs121918618
geneview	rs121918618
scholar	rs121918618
google	rs121918618
pharmgkb	rs121918618
gwascentral	rs121918618
openSNP	rs121918618
23andMe	rs121918618
SNPshot	rs121918618
SNPdbe	rs121918618
MSV3d	rs121918618
GWAS Ctlg	rs121918618

Max Magnitude

0

OMIM	182340
Desc
Variant	0012
Related	also

ClinVar
Risk	rs121918618(T;T)
Alt	rs121918618(T;T)
Reference	Rs121918618(C;C)
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.160098797C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013791.26,