rs28933398

Orientation

plus

Stabilized

plus

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

Make rs28933398(C;C)

Make rs28933398(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160135845

Gene

ATP1A2

is a	snp
is	mentioned by
dbSNP	rs28933398
dbSNP (classic)	rs28933398
ClinGen	rs28933398
ebi	rs28933398
HLI	rs28933398
Exac	rs28933398
Gnomad	rs28933398
Varsome	rs28933398
LitVar	rs28933398
Map	rs28933398
PheGenI	rs28933398
Biobank	rs28933398
1000 genomes	rs28933398
hgdp	rs28933398
ensembl	rs28933398
geneview	rs28933398
scholar	rs28933398
google	rs28933398
pharmgkb	rs28933398
gwascentral	rs28933398
openSNP	rs28933398
23andMe	rs28933398
SNPshot	rs28933398
SNPdbe	rs28933398
MSV3d	rs28933398
GWAS Ctlg	rs28933398

Max Magnitude

0

OMIM	182340
Desc	MIGRAINE, FAMILIAL HEMIPLEGIC, 2
Variant	0001
Related	also

ClinVar
Risk	rs28933398(C;C)
Alt	rs28933398(C;C)
Reference	Rs28933398(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.160105635T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013780.25,