rs386134186

Orientation

minus

Stabilized

minus

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

Make rs386134186(C;C)

Make rs386134186(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

201723325

Gene

ALS2

is a	snp
is	mentioned by
dbSNP	rs386134186
dbSNP (classic)	rs386134186
ClinGen	rs386134186
ebi	rs386134186
HLI	rs386134186
Exac	rs386134186
Gnomad	rs386134186
Varsome	rs386134186
LitVar	rs386134186
Map	rs386134186
PheGenI	rs386134186
Biobank	rs386134186
1000 genomes	rs386134186
hgdp	rs386134186
ensembl	rs386134186
geneview	rs386134186
scholar	rs386134186
google	rs386134186
pharmgkb	rs386134186
gwascentral	rs386134186
openSNP	rs386134186
23andMe	rs386134186
SNPshot	rs386134186
SNPdbe	rs386134186
MSV3d	rs386134186
GWAS Ctlg	rs386134186

Max Magnitude

0

ClinVar
Risk	rs386134186(C;C)
Alt	rs386134186(C;C)
Reference	Rs386134186(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.202588048C>G
CLNSRC
CLNACC	RCV000034989.1,