rs730882255

Orientation

minus

Stabilized

minus

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

Make rs730882255(G;T)

Make rs730882255(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

201744426

Gene

ALS2

is a	snp
is	mentioned by
dbSNP	rs730882255
dbSNP (classic)	rs730882255
ClinGen	rs730882255
ebi	rs730882255
HLI	rs730882255
Exac	rs730882255
Gnomad	rs730882255
Varsome	rs730882255
LitVar	rs730882255
Map	rs730882255
PheGenI	rs730882255
Biobank	rs730882255
1000 genomes	rs730882255
hgdp	rs730882255
ensembl	rs730882255
geneview	rs730882255
scholar	rs730882255
google	rs730882255
pharmgkb	rs730882255
gwascentral	rs730882255
openSNP	rs730882255
23andMe	rs730882255
SNPshot	rs730882255
SNPdbe	rs730882255
MSV3d	rs730882255
GWAS Ctlg	rs730882255

Max Magnitude

0

ClinVar
Risk	rs730882255(T;T)
Alt	rs730882255(T;T)
Reference	Rs730882255(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.202609149C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000162071.3,