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rs121909669

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909669(A;A)
Make rs121909669(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position31191410
GeneFUS
is asnp
is mentioned by
dbSNPrs121909669
ebirs121909669
HLIrs121909669
Exacrs121909669
Varsomers121909669
Maprs121909669
PheGenIrs121909669
hapmaprs121909669
1000 genomesrs121909669
hgdprs121909669
ensemblrs121909669
gopubmedrs121909669
geneviewrs121909669
scholarrs121909669
googlers121909669
pharmgkbrs121909669
gwascentralrs121909669
openSNPrs121909669
23andMers121909669
23andMe allrs121909669
SNP Nexus

SNPshotrs121909669
SNPdbers121909669
MSV3drs121909669
GWAS Ctlgrs121909669
Max Magnitude0
OMIM137070
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909669(A;A)
Alt rs121909669(A;A)
Reference rs121909669(G;G)
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.31202731G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017610.27,