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rs6587852

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs6587852(A;A)
Make rs6587852(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position59239775
is asnp
is mentioned by
dbSNPrs6587852
ebirs6587852
HLIrs6587852
Exacrs6587852
Varsomers6587852
Maprs6587852
PheGenIrs6587852
hapmaprs6587852
1000 genomesrs6587852
hgdprs6587852
ensemblrs6587852
gopubmedrs6587852
geneviewrs6587852
scholarrs6587852
googlers6587852
pharmgkbrs6587852
gwascentralrs6587852
openSNPrs6587852
23andMers6587852
23andMe allrs6587852
SNP Nexus

SNPshotrs6587852
SNPdbers6587852
MSV3drs6587852
GWAS Ctlgrs6587852
GMAF0.225
Max Magnitude0
? (A;A) (A;C) (C;C) 28
rs6587852 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