rs398122926

Orientation

plus

Stabilized

plus

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

Make rs398122926(-;T)

Make rs398122926(T;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

11753835

Gene

GNAL

is a	snp
is	mentioned by
dbSNP	rs398122926
dbSNP (classic)	rs398122926
ClinGen	rs398122926
ebi	rs398122926
HLI	rs398122926
Exac	rs398122926
Gnomad	rs398122926
Varsome	rs398122926
LitVar	rs398122926
Map	rs398122926
PheGenI	rs398122926
Biobank	rs398122926
1000 genomes	rs398122926
hgdp	rs398122926
ensembl	rs398122926
geneview	rs398122926
scholar	rs398122926
google	rs398122926
pharmgkb	rs398122926
gwascentral	rs398122926
openSNP	rs398122926
23andMe	rs398122926
SNPshot	rs398122926
SNPdbe	rs398122926
MSV3d	rs398122926
GWAS Ctlg	rs398122926

Max Magnitude

0

ClinVar
Risk	rs398122926(T;T)
Alt	rs398122926(T;T)
Reference	Rs398122926(-;-)
Significance	Pathogenic
Disease	Dystonia 25
Variation	info
Gene	GNAL
CLNDBN	Dystonia 25
Reversed	0
HGVS	NC_000018.9:g.11753834dupT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000033104.24,