rs121918616

Orientation

plus

Stabilized

plus

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

Make rs121918616(A;A)

Make rs121918616(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160130283

Gene

ATP1A2

is a	snp
is	mentioned by
dbSNP	rs121918616
dbSNP (classic)	rs121918616
ClinGen	rs121918616
ebi	rs121918616
HLI	rs121918616
Exac	rs121918616
Gnomad	rs121918616
Varsome	rs121918616
LitVar	rs121918616
Map	rs121918616
PheGenI	rs121918616
Biobank	rs121918616
1000 genomes	rs121918616
hgdp	rs121918616
ensembl	rs121918616
geneview	rs121918616
scholar	rs121918616
google	rs121918616
pharmgkb	rs121918616
gwascentral	rs121918616
openSNP	rs121918616
23andMe	rs121918616
SNPshot	rs121918616
SNPdbe	rs121918616
MSV3d	rs121918616
GWAS Ctlg	rs121918616

Max Magnitude

0

OMIM	182340
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121918616(A;A)
Alt	rs121918616(A;A)
Reference	Rs121918616(G;G)
Significance	Pathogenic
Disease	Migraine not provided
Variation	info
Gene	ATP1A2
CLNDBN	Migraine, familial basilar not provided
Reversed	0
HGVS	NC_000001.10:g.160100073G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013789.18, RCV000423537.1,