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rs2151145

From SNPedia

Orientationminus
Stabilizedminus
Make rs2151145(C;C)
Make rs2151145(C;T)
Make rs2151145(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position79730966
is asnp
is mentioned by
dbSNPrs2151145
ClinGenrs2151145
ebirs2151145
HLIrs2151145
Exacrs2151145
Varsomers2151145
Maprs2151145
PheGenIrs2151145
hapmaprs2151145
1000 genomesrs2151145
hgdprs2151145
ensemblrs2151145
gopubmedrs2151145
geneviewrs2151145
scholarrs2151145
googlers2151145
pharmgkbrs2151145
gwascentralrs2151145
openSNPrs2151145
23andMers2151145
23andMe allrs2151145
SNP Nexus

SNPshotrs2151145
SNPdbers2151145
MSV3drs2151145
GWAS Ctlgrs2151145
GMAF0.2029
Max Magnitude
? (C;C) (C;T) (T;T) 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 1E-7
Odds Ratio 0.41 [0.26-0.56] years older


GET Evidence
rs2151145
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.811475
summary