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rs17188434

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs17188434(C;C)
Make rs17188434(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position156240264
GeneLINC01876
is asnp
is mentioned by
dbSNPrs17188434
dbSNP (classic)rs17188434
ClinGenrs17188434
ebirs17188434
HLIrs17188434
Exacrs17188434
Gnomadrs17188434
Varsomers17188434
LitVarrs17188434
Maprs17188434
PheGenIrs17188434
Biobankrs17188434
1000 genomesrs17188434
hgdprs17188434
ensemblrs17188434
geneviewrs17188434
scholarrs17188434
googlers17188434
pharmgkbrs17188434
gwascentralrs17188434
openSNPrs17188434
23andMers17188434
SNPshotrs17188434
SNPdbers17188434
MSV3drs17188434
GWAS Ctlgrs17188434
GMAF0.02847
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 21102462OA-icon.png]
Trait
Title Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Risk Allele C
P-val 1E-9
Odds Ratio 4.5000 [3.13-5.87] week decrease