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rs121909671

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909671(A;A)
Make rs121909671(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position31191419
GeneFUS
is asnp
is mentioned by
dbSNPrs121909671
ebirs121909671
HLIrs121909671
Exacrs121909671
Varsomers121909671
Maprs121909671
PheGenIrs121909671
hapmaprs121909671
1000 genomesrs121909671
hgdprs121909671
ensemblrs121909671
gopubmedrs121909671
geneviewrs121909671
scholarrs121909671
googlers121909671
pharmgkbrs121909671
gwascentralrs121909671
openSNPrs121909671
23andMers121909671
23andMe allrs121909671
SNP Nexus

SNPshotrs121909671
SNPdbers121909671
MSV3drs121909671
GWAS Ctlgrs121909671
Max Magnitude0
OMIM137070
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909671(A;A)
Alt rs121909671(A;A)
Reference rs121909671(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.31202740G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017612.27,