rs28933401

Orientation

plus

Stabilized

plus

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

Make rs28933401(A;A)

Make rs28933401(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160135246

Gene

ATP1A2

is a	snp
is	mentioned by
dbSNP	rs28933401
dbSNP (classic)	rs28933401
ClinGen	rs28933401
ebi	rs28933401
HLI	rs28933401
Exac	rs28933401
Gnomad	rs28933401
Varsome	rs28933401
LitVar	rs28933401
Map	rs28933401
PheGenI	rs28933401
Biobank	rs28933401
1000 genomes	rs28933401
hgdp	rs28933401
ensembl	rs28933401
geneview	rs28933401
scholar	rs28933401
google	rs28933401
pharmgkb	rs28933401
gwascentral	rs28933401
openSNP	rs28933401
23andMe	rs28933401
SNPshot	rs28933401
SNPdbe	rs28933401
MSV3d	rs28933401
GWAS Ctlg	rs28933401

Max Magnitude

0

OMIM	182340
Desc	MIGRAINE, FAMILIAL HEMIPLEGIC, 2
Variant	0004
Related	also

ClinVar
Risk	rs28933401(A;A)
Alt	rs28933401(A;A)
Reference	Rs28933401(G;G)
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.160105036G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013783.19,