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rs121909670

From SNPedia

Merged intors121909668
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909670(C;T)
Make rs121909670(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position31191418
GeneFUS
is asnp
is mentioned by
dbSNPrs121909670
ebirs121909670
HLIrs121909670
Exacrs121909670
Varsomers121909670
Maprs121909670
PheGenIrs121909670
hapmaprs121909670
1000 genomesrs121909670
hgdprs121909670
ensemblrs121909670
gopubmedrs121909670
geneviewrs121909670
scholarrs121909670
googlers121909670
pharmgkbrs121909670
gwascentralrs121909670
openSNPrs121909670
23andMers121909670
23andMe allrs121909670
SNP Nexus

SNPshotrs121909670
SNPdbers121909670
MSV3drs121909670
GWAS Ctlgrs121909670
StatusMerged into rs121909668
Max Magnitude0
OMIM137070
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909670(T;T)
Alt rs121909670(T;T)
Reference rs121909670(C;C)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis type 6
Variation info
Gene FUS
CLNDBN Amyotrophic lateral sclerosis type 6
Reversed 0
HGVS NC_000016.9:g.31202739C>T
CLNSRC OMIM Allelic Variant
CLNACC SCV000037884.1,