rs28933400

Orientation

plus

Stabilized

plus

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

Make rs28933400(C;C)

Make rs28933400(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160135510

Gene

ATP1A2

is a	snp
is	mentioned by
dbSNP	rs28933400
dbSNP (classic)	rs28933400
ClinGen	rs28933400
ebi	rs28933400
HLI	rs28933400
Exac	rs28933400
Gnomad	rs28933400
Varsome	rs28933400
LitVar	rs28933400
Map	rs28933400
PheGenI	rs28933400
Biobank	rs28933400
1000 genomes	rs28933400
hgdp	rs28933400
ensembl	rs28933400
geneview	rs28933400
scholar	rs28933400
google	rs28933400
pharmgkb	rs28933400
gwascentral	rs28933400
openSNP	rs28933400
23andMe	rs28933400
SNPshot	rs28933400
SNPdbe	rs28933400
MSV3d	rs28933400
GWAS Ctlg	rs28933400

Max Magnitude

0

OMIM	182340
Desc	MIGRAINE, FAMILIAL HEMIPLEGIC, 2
Variant	0003
Related	also

ClinVar
Risk	rs28933400(C;C)
Alt	rs28933400(C;C)
Reference	Rs28933400(T;T)
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.160105300T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013782.24,

[PMID 19199261] [Association of the polymorphisms of sodium transport related genes with essential hypertension].