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rs7861820

From SNPedia

Orientationplus
Stabilizedplus
Make rs7861820(C;C)
Make rs7861820(C;T)
Make rs7861820(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position106174393
is asnp
is mentioned by
dbSNPrs7861820
ebirs7861820
HLIrs7861820
Exacrs7861820
Varsomers7861820
Maprs7861820
PheGenIrs7861820
hapmaprs7861820
1000 genomesrs7861820
hgdprs7861820
ensemblrs7861820
gopubmedrs7861820
geneviewrs7861820
scholarrs7861820
googlers7861820
pharmgkbrs7861820
gwascentralrs7861820
openSNPrs7861820
23andMers7861820
23andMe allrs7861820
SNP Nexus

SNPshotrs7861820
SNPdbers7861820
MSV3drs7861820
GWAS Ctlgrs7861820
GMAF0.3365
Max Magnitude
? (C;C) (C;T) (T;T) 28

23andMe blog rs7861820(C) about five weeks earlier menarche.

GWAS snp
PMID [PMID 19448621OA-icon.png]
Trait Menarche and menopause (age at onset)
Title Genome-wide association studies identify loci associated with age at menarche and age at natural menopause
Risk Allele C
P-val 3E-9
Odds Ratio 0.09 [0.06-0.12] years younger
OMIM612883
Desc
Variant
Relatedalso


GET Evidence
rs7861820
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.671875
summary