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rs730882255

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730882255(G;T)
Make rs730882255(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position201744426
GeneALS2
is asnp
is mentioned by
dbSNPrs730882255
ebirs730882255
HLIrs730882255
Exacrs730882255
Varsomers730882255
Maprs730882255
PheGenIrs730882255
hapmaprs730882255
1000 genomesrs730882255
hgdprs730882255
ensemblrs730882255
gopubmedrs730882255
geneviewrs730882255
scholarrs730882255
googlers730882255
pharmgkbrs730882255
gwascentralrs730882255
openSNPrs730882255
23andMers730882255
23andMe allrs730882255
SNP Nexus

SNPshotrs730882255
SNPdbers730882255
MSV3drs730882255
GWAS Ctlgrs730882255
Max Magnitude0
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,