rs730882256

Orientation

minus

Stabilized

minus

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

Make rs730882256(-;G)

Make rs730882256(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

201706852

Gene

ALS2

is a	snp
is	mentioned by
dbSNP	rs730882256
dbSNP (classic)	rs730882256
ClinGen	rs730882256
ebi	rs730882256
HLI	rs730882256
Exac	rs730882256
Gnomad	rs730882256
Varsome	rs730882256
LitVar	rs730882256
Map	rs730882256
PheGenI	rs730882256
Biobank	rs730882256
1000 genomes	rs730882256
hgdp	rs730882256
ensembl	rs730882256
geneview	rs730882256
scholar	rs730882256
google	rs730882256
pharmgkb	rs730882256
gwascentral	rs730882256
openSNP	rs730882256
23andMe	rs730882256
SNPshot	rs730882256
SNPdbe	rs730882256
MSV3d	rs730882256
GWAS Ctlg	rs730882256

Max Magnitude

0

ClinVar
Risk	rs730882256(G;G)
Alt	rs730882256(G;G)
Reference	Rs730882256(-;-)
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.202571576dupC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000162072.3,