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rs17153527

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs17153527(C;C)
Make rs17153527(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position106855364
is asnp
is mentioned by
dbSNPrs17153527
ebirs17153527
HLIrs17153527
Exacrs17153527
Varsomers17153527
Maprs17153527
PheGenIrs17153527
hapmaprs17153527
1000 genomesrs17153527
hgdprs17153527
ensemblrs17153527
gopubmedrs17153527
geneviewrs17153527
scholarrs17153527
googlers17153527
pharmgkbrs17153527
gwascentralrs17153527
openSNPrs17153527
23andMers17153527
23andMe allrs17153527
SNP Nexus

SNPshotrs17153527
SNPdbers17153527
MSV3drs17153527
GWAS Ctlgrs17153527
GMAF0.1047
Max Magnitude0
? (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 4E-7
Odds Ratio 0.51 [0.31-0.71] years older


GET Evidence
rs17153527
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0625
summary