rs121918615

Orientation

plus

Stabilized

plus

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

Make rs121918615(C;T)

Make rs121918615(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160139735

Gene

ATP1A2

is a	snp
is	mentioned by
dbSNP	rs121918615
dbSNP (classic)	rs121918615
ClinGen	rs121918615
ebi	rs121918615
HLI	rs121918615
Exac	rs121918615
Gnomad	rs121918615
Varsome	rs121918615
LitVar	rs121918615
Map	rs121918615
PheGenI	rs121918615
Biobank	rs121918615
1000 genomes	rs121918615
hgdp	rs121918615
ensembl	rs121918615
geneview	rs121918615
scholar	rs121918615
google	rs121918615
pharmgkb	rs121918615
gwascentral	rs121918615
openSNP	rs121918615
23andMe	rs121918615
SNPshot	rs121918615
SNPdbe	rs121918615
MSV3d	rs121918615
GWAS Ctlg	rs121918615

Max Magnitude

0

OMIM	182340
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121918615(T;T)
Alt	rs121918615(T;T)
Reference	Rs121918615(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.160109525C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013788.26,