rs398122925

Orientation

plus

Stabilized

plus

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

Make rs398122925(A;A)

Make rs398122925(A;G)

Reference

GRCh38 38.1/141

Chromosome

18

Position

11824987

Gene

GNAL

is a	snp
is	mentioned by
dbSNP	rs398122925
dbSNP (classic)	rs398122925
ClinGen	rs398122925
ebi	rs398122925
HLI	rs398122925
Exac	rs398122925
Gnomad	rs398122925
Varsome	rs398122925
LitVar	rs398122925
Map	rs398122925
PheGenI	rs398122925
Biobank	rs398122925
1000 genomes	rs398122925
hgdp	rs398122925
ensembl	rs398122925
geneview	rs398122925
scholar	rs398122925
google	rs398122925
pharmgkb	rs398122925
gwascentral	rs398122925
openSNP	rs398122925
23andMe	rs398122925
SNPshot	rs398122925
SNPdbe	rs398122925
MSV3d	rs398122925
GWAS Ctlg	rs398122925

Max Magnitude

0

ClinVar
Risk	rs398122925(A;A)
Alt	rs398122925(A;A)
Reference	Rs398122925(G;G)
Significance	Pathogenic
Disease	Dystonia 25
Variation	info
Gene	GNAL
CLNDBN	Dystonia 25
Reversed	0
HGVS	NC_000018.9:g.11824986G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000033103.26,