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rs1455311

From SNPedia

Orientationminus
Stabilizedminus
Make rs1455311(C;C)
Make rs1455311(C;T)
Make rs1455311(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position79043433
GeneLINC01088
is asnp
is mentioned by
dbSNPrs1455311
dbSNP (classic)rs1455311
ClinGenrs1455311
ebirs1455311
HLIrs1455311
Exacrs1455311
Gnomadrs1455311
Varsomers1455311
LitVarrs1455311
Maprs1455311
PheGenIrs1455311
Biobankrs1455311
1000 genomesrs1455311
hgdprs1455311
ensemblrs1455311
geneviewrs1455311
scholarrs1455311
googlers1455311
pharmgkbrs1455311
gwascentralrs1455311
openSNPrs1455311
23andMers1455311
SNPshotrs1455311
SNPdbers1455311
MSV3drs1455311
GWAS Ctlgrs1455311
GMAF0.1364
Max Magnitude0
? (C;C) (C;T) (T;T) 28


Newsweek has reported in the article The Little Flaw in the Longevity-Gene Study That Could Be a Big Problem that the associations for rs1036819 and rs1455311 may be incorrect because of a flaw in one of the chips used. Mentioned in retracted [PMID 20595579]


[PMID 22105264OA-icon.png] Identification of six Loci associated with pelvic organ prolapse using genome-wide association analysis