rs398122927

Orientation

plus

Stabilized

plus

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

Make rs398122927(-;A)

Make rs398122927(A;A)

Reference

GRCh38 38.1/141

Chromosome

18

Position

11864577

Gene

GNAL

is a	snp
is	mentioned by
dbSNP	rs398122927
dbSNP (classic)	rs398122927
ClinGen	rs398122927
ebi	rs398122927
HLI	rs398122927
Exac	rs398122927
Gnomad	rs398122927
Varsome	rs398122927
LitVar	rs398122927
Map	rs398122927
PheGenI	rs398122927
Biobank	rs398122927
1000 genomes	rs398122927
hgdp	rs398122927
ensembl	rs398122927
geneview	rs398122927
scholar	rs398122927
google	rs398122927
pharmgkb	rs398122927
gwascentral	rs398122927
openSNP	rs398122927
23andMe	rs398122927
SNPshot	rs398122927
SNPdbe	rs398122927
MSV3d	rs398122927
GWAS Ctlg	rs398122927

Max Magnitude

0

ClinVar
Risk	rs398122927(A;A)
Alt	rs398122927(A;A)
Reference	Rs398122927(-;-)
Significance	Pathogenic
Disease	Dystonia 25
Variation	info
Gene	GNAL
CLNDBN	Dystonia 25
Reversed	0
HGVS	NC_000018.9:g.11864576dupA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000033105.24,