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

rs333662

From SNPedia

Orientationminus
Stabilizedminus
Make rs333662(C;C)
Make rs333662(C;T)
Make rs333662(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position59278242
is asnp
is mentioned by
dbSNPrs333662
ebirs333662
HLIrs333662
Exacrs333662
Varsomers333662
Maprs333662
PheGenIrs333662
hapmaprs333662
1000 genomesrs333662
hgdprs333662
ensemblrs333662
gopubmedrs333662
geneviewrs333662
scholarrs333662
googlers333662
pharmgkbrs333662
gwascentralrs333662
openSNPrs333662
23andMers333662
23andMe allrs333662
SNP Nexus

SNPshotrs333662
SNPdbers333662
MSV3drs333662
GWAS Ctlgrs333662
GMAF0.1488
Max Magnitude
? (C;C) (C;T) (T;T) 28
rs333662 is one of 6 SNPs found upstream of an (uncharacterized) gene known as FLJ10986 that have been found to be overrepresented in 1,152 patients with sporadic amyotrophic lateral sclerosis (ALS).[PMID 17671248]

[PMID 19177248] A study involving a large case-control series from the Netherlands, Belgium, Sweden and Ireland (total: 1883 sporadic ALS patients and 2063 controls) found no significant association between sporadic ALS and the six previously reported associated SNPs, including this one.


[PMID 19922138] Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis