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rs121912458

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121912458(A;G)
Make rs121912458(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position31667260
GeneSOD1
is asnp
is mentioned by
dbSNPrs121912458
ebirs121912458
HLIrs121912458
Exacrs121912458
Varsomers121912458
Maprs121912458
PheGenIrs121912458
hapmaprs121912458
1000 genomesrs121912458
hgdprs121912458
ensemblrs121912458
gopubmedrs121912458
geneviewrs121912458
scholarrs121912458
googlers121912458
pharmgkbrs121912458
gwascentralrs121912458
openSNPrs121912458
23andMers121912458
23andMe allrs121912458
SNP Nexus

SNPshotrs121912458
SNPdbers121912458
MSV3drs121912458
GWAS Ctlgrs121912458
Max Magnitude0
OMIM147450
Desc
Variant0031
Relatedalso
ClinVar
Risk rs121912458(G;G)
Alt rs121912458(G;G)
Reference rs121912458(A;A)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis type 1
Variation info
Gene SOD1
CLNDBN Amyotrophic lateral sclerosis type 1
Reversed 0
HGVS NC_000021.8:g.33039573A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000015905.27,