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rs17880487

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17880487(C;T)
Make rs17880487(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position31668917
GeneSOD1
is asnp
is mentioned by
dbSNPrs17880487
dbSNP (classic)rs17880487
ClinGenrs17880487
ebirs17880487
HLIrs17880487
Exacrs17880487
Gnomadrs17880487
Varsomers17880487
LitVarrs17880487
Maprs17880487
PheGenIrs17880487
Biobankrs17880487
1000 genomesrs17880487
hgdprs17880487
ensemblrs17880487
geneviewrs17880487
scholarrs17880487
googlers17880487
pharmgkbrs17880487
gwascentralrs17880487
openSNPrs17880487
23andMers17880487
SNPshotrs17880487
SNPdbers17880487
MSV3drs17880487
GWAS Ctlgrs17880487
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 27755600OA-icon.png] The Impact of Superoxide Dismutase-1 Genetic Variation on Cardiovascular and All-Cause Mortality in a Prospective Cohort Study: The Yamagata (Takahata) Study.


ClinVar
Risk rs17880487(T;T)
Alt rs17880487(T;T)
Reference Rs17880487(C;C)
Significance Probable-non-pathogenic
Disease Amyotrophic Lateral Sclerosis
Variation info
Gene SOD1
CLNDBN Amyotrophic Lateral Sclerosis, Dominant
Reversed 0
HGVS NC_000021.8:g.33041230C>T
CLNSRC
CLNACC RCV000407681.1,