rs398122924

Orientation

plus

Stabilized

plus

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

Make rs398122924(A;A)

Make rs398122924(A;C)

Reference

GRCh38 38.1/141

Chromosome

18

Position

11872345

Gene

GNAL

is a	snp
is	mentioned by
dbSNP	rs398122924
dbSNP (classic)	rs398122924
ClinGen	rs398122924
ebi	rs398122924
HLI	rs398122924
Exac	rs398122924
Gnomad	rs398122924
Varsome	rs398122924
LitVar	rs398122924
Map	rs398122924
PheGenI	rs398122924
Biobank	rs398122924
1000 genomes	rs398122924
hgdp	rs398122924
ensembl	rs398122924
geneview	rs398122924
scholar	rs398122924
google	rs398122924
pharmgkb	rs398122924
gwascentral	rs398122924
openSNP	rs398122924
23andMe	rs398122924
SNPshot	rs398122924
SNPdbe	rs398122924
MSV3d	rs398122924
GWAS Ctlg	rs398122924

Max Magnitude

0

ClinVar
Risk	rs398122924(A;A)
Alt	rs398122924(A;A)
Reference	Rs398122924(C;C)
Significance	Pathogenic
Disease	Dystonia 25
Variation	info
Gene	GNAL
CLNDBN	Dystonia 25
Reversed	0
HGVS	NC_000018.9:g.11872344C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000033102.26,