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rs730882256

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730882256(-;-)
Make rs730882256(-;G)
Make rs730882256(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position201706852
GeneALS2
is asnp
is mentioned by
dbSNPrs730882256
ebirs730882256
HLIrs730882256
Exacrs730882256
Varsomers730882256
Maprs730882256
PheGenIrs730882256
hapmaprs730882256
1000 genomesrs730882256
hgdprs730882256
ensemblrs730882256
gopubmedrs730882256
geneviewrs730882256
scholarrs730882256
googlers730882256
pharmgkbrs730882256
gwascentralrs730882256
openSNPrs730882256
23andMers730882256
23andMe allrs730882256
SNP Nexus

SNPshotrs730882256
SNPdbers730882256
MSV3drs730882256
GWAS Ctlgrs730882256
Max Magnitude0
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,