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rs121909668

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909668(C;G)
Make rs121909668(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position31191418
GeneFUS
is asnp
is mentioned by
dbSNPrs121909668
ebirs121909668
HLIrs121909668
Exacrs121909668
Varsomers121909668
Maprs121909668
PheGenIrs121909668
hapmaprs121909668
1000 genomesrs121909668
hgdprs121909668
ensemblrs121909668
gopubmedrs121909668
geneviewrs121909668
scholarrs121909668
googlers121909668
pharmgkbrs121909668
gwascentralrs121909668
openSNPrs121909668
23andMers121909668
23andMe allrs121909668
SNP Nexus

SNPshotrs121909668
SNPdbers121909668
MSV3drs121909668
GWAS Ctlgrs121909668
Merged fromRs121909670
Max Magnitude0
OMIM137070
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909668(G;G) rs121909668(T;T)
Alt rs121909668(G;G) rs121909668(T;T)
Reference Rs121909668(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>G; NC_000016.9:g.31202739C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000017609.27, RCV000017611.25,