rs386134185

Orientation

minus

Stabilized

minus

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

Make rs386134185(-;-)

Make rs386134185(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

201723389

Gene

ALS2

is a	snp
is	mentioned by
dbSNP	rs386134185
dbSNP (classic)	rs386134185
ClinGen	rs386134185
ebi	rs386134185
HLI	rs386134185
Exac	rs386134185
Gnomad	rs386134185
Varsome	rs386134185
LitVar	rs386134185
Map	rs386134185
PheGenI	rs386134185
Biobank	rs386134185
1000 genomes	rs386134185
hgdp	rs386134185
ensembl	rs386134185
geneview	rs386134185
scholar	rs386134185
google	rs386134185
pharmgkb	rs386134185
gwascentral	rs386134185
openSNP	rs386134185
23andMe	rs386134185
SNPshot	rs386134185
SNPdbe	rs386134185
MSV3d	rs386134185
GWAS Ctlg	rs386134185

Max Magnitude

0

ClinVar
Risk	rs386134185(-;-)
Alt	rs386134185(-;-)
Reference	Rs386134185(G;G)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 2
Variation	info
Gene	ALS2
CLNDBN	Amyotrophic lateral sclerosis type 2
Reversed	1
HGVS	NC_000002.11:g.202588112delC
CLNSRC
CLNACC	RCV000034989.1,