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rs929867

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs929867(C;C)
Make rs929867(C;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position31180161
GeneFUS
is asnp
is mentioned by
dbSNPrs929867
dbSNP (old)rs929867
ClinGenrs929867
ebirs929867
HLIrs929867
Exacrs929867
Gnomadrs929867
Varsomers929867
Maprs929867
PheGenIrs929867
Biobankrs929867
1000 genomesrs929867
hgdprs929867
ensemblrs929867
gopubmedrs929867
geneviewrs929867
scholarrs929867
googlers929867
pharmgkbrs929867
gwascentralrs929867
openSNPrs929867
23andMers929867
23andMe allrs929867
SNP Nexus

SNPshotrs929867
SNPdbers929867
MSV3drs929867
GWAS Ctlgrs929867
Max Magnitude0
Although based on a relatively small study, there's a strong association (odds ratios above 30) between the very rare (and neighboring) minor alleles of rs8056264 and rs929867 with common variable immunodeficiency (CVID) reported in [PMID 25678086OA-icon.png].


ClinVar
Risk rs929867(C;C)
Alt rs929867(C;C)
Reference Rs929867(T;T)
Significance Non-pathogenic
Disease Amyotrophic Lateral Sclerosis
Variation info
Gene FUS
CLNDBN Amyotrophic Lateral Sclerosis, Dominant
Reversed 1
HGVS NC_000016.9:g.31191482A>G
CLNSRC
CLNACC RCV000307180.1,