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rs4906172

From SNPedia

Orientationplus
Stabilizedplus
Make rs4906172(A;A)
Make rs4906172(A;C)
Make rs4906172(C;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position101988596
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs4906172
ebirs4906172
HLIrs4906172
Exacrs4906172
Varsomers4906172
Maprs4906172
PheGenIrs4906172
hapmaprs4906172
1000 genomesrs4906172
hgdprs4906172
ensemblrs4906172
gopubmedrs4906172
geneviewrs4906172
scholarrs4906172
googlers4906172
pharmgkbrs4906172
gwascentralrs4906172
openSNPrs4906172
23andMers4906172
23andMe allrs4906172
SNP Nexus

SNPshotrs4906172
SNPdbers4906172
MSV3drs4906172
GWAS Ctlgrs4906172
GMAF0.3517
Max Magnitude
? (A;A) (A;C) (C;C) 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 0.000003
Odds Ratio 0.36 [0.21-0.51] years younger


GET Evidence
rs4906172
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.421875
summary