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rs4955755

From SNPedia

Orientationplus
Stabilizedplus
Make rs4955755(A;A)
Make rs4955755(A;G)
Make rs4955755(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position170776620
is asnp
is mentioned by
dbSNPrs4955755
ebirs4955755
HLIrs4955755
Exacrs4955755
Varsomers4955755
Maprs4955755
PheGenIrs4955755
hapmaprs4955755
1000 genomesrs4955755
hgdprs4955755
ensemblrs4955755
gopubmedrs4955755
geneviewrs4955755
scholarrs4955755
googlers4955755
pharmgkbrs4955755
gwascentralrs4955755
openSNPrs4955755
23andMers4955755
23andMe allrs4955755
SNP Nexus

SNPshotrs4955755
SNPdbers4955755
MSV3drs4955755
GWAS Ctlgrs4955755
GMAF0.4848
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 7E-7
Odds Ratio 0.34 [0.21-0.47] years older


GET Evidence
rs4955755
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.492188
summary