rs398122928

Orientation

plus

Stabilized

plus

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

Make rs398122928(C;T)

Make rs398122928(T;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

11752494

Gene

GNAL

is a	snp
is	mentioned by
dbSNP	rs398122928
dbSNP (classic)	rs398122928
ClinGen	rs398122928
ebi	rs398122928
HLI	rs398122928
Exac	rs398122928
Gnomad	rs398122928
Varsome	rs398122928
LitVar	rs398122928
Map	rs398122928
PheGenI	rs398122928
Biobank	rs398122928
1000 genomes	rs398122928
hgdp	rs398122928
ensembl	rs398122928
geneview	rs398122928
scholar	rs398122928
google	rs398122928
pharmgkb	rs398122928
gwascentral	rs398122928
openSNP	rs398122928
23andMe	rs398122928
SNPshot	rs398122928
SNPdbe	rs398122928
MSV3d	rs398122928
GWAS Ctlg	rs398122928

Max Magnitude

0

ClinVar
Risk	rs398122928(T;T)
Alt	rs398122928(T;T)
Reference	Rs398122928(C;C)
Significance	Pathogenic
Disease	Dystonia 25
Variation	info
Gene	GNAL
CLNDBN	Dystonia 25
Reversed	0
HGVS	NC_000018.9:g.11752493C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000033106.26,