Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606831

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606831(A;A)
Make rs267606831(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position31191089
GeneFUS
is asnp
is mentioned by
dbSNPrs267606831
ebirs267606831
HLIrs267606831
Exacrs267606831
Varsomers267606831
Maprs267606831
PheGenIrs267606831
hapmaprs267606831
1000 genomesrs267606831
hgdprs267606831
ensemblrs267606831
gopubmedrs267606831
geneviewrs267606831
scholarrs267606831
googlers267606831
pharmgkbrs267606831
gwascentralrs267606831
openSNPrs267606831
23andMers267606831
23andMe allrs267606831
SNP Nexus

SNPshotrs267606831
SNPdbers267606831
MSV3drs267606831
GWAS Ctlgrs267606831
Max Magnitude0
ClinVar
Risk rs267606831(A;A)
Alt rs267606831(A;A)
Reference rs267606831(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.31202410G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017613.23,