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rs11889862

From SNPedia

Orientationplus
Stabilizedplus
Make rs11889862(A;A)
Make rs11889862(A;G)
Make rs11889862(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position149840634
GeneTOLLIP
is asnp
is mentioned by
dbSNPrs11889862
ebirs11889862
HLIrs11889862
Exacrs11889862
Varsomers11889862
Maprs11889862
PheGenIrs11889862
hapmaprs11889862
1000 genomesrs11889862
hgdprs11889862
ensemblrs11889862
gopubmedrs11889862
geneviewrs11889862
scholarrs11889862
googlers11889862
pharmgkbrs11889862
gwascentralrs11889862
openSNPrs11889862
23andMers11889862
23andMe allrs11889862
SNP Nexus

SNPshotrs11889862
SNPdbers11889862
MSV3drs11889862
GWAS Ctlgrs11889862
GMAF0.2874
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19448619OA-icon.png]
Trait Menopause
Title Loci at chromosomes 13, 19 and 20 influence age at natural menopause.
Risk Allele
P-val 0.000002
Odds Ratio 0.36 [0.21-0.51] years younger


GET Evidence
rs11889862
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.733333
summary