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rs9814870

From SNPedia

Orientationplus
Stabilizedplus
Make rs9814870(A;A)
Make rs9814870(A;G)
Make rs9814870(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position95969999
is asnp
is mentioned by
dbSNPrs9814870
ebirs9814870
HLIrs9814870
Exacrs9814870
Varsomers9814870
Maprs9814870
PheGenIrs9814870
hapmaprs9814870
1000 genomesrs9814870
hgdprs9814870
ensemblrs9814870
gopubmedrs9814870
geneviewrs9814870
scholarrs9814870
googlers9814870
pharmgkbrs9814870
gwascentralrs9814870
openSNPrs9814870
23andMers9814870
23andMe allrs9814870
SNP Nexus

SNPshotrs9814870
SNPdbers9814870
MSV3drs9814870
GWAS Ctlgrs9814870
GMAF0.1781
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19478329]
Trait Male infertility
Title Genome-wide Study of Single Nucleotide Polymorphisms Associated with Azoospermia and Severe Oligozoospermia
Risk Allele
P-val 7E-7
Odds Ratio NR NR


GET Evidence
rs9814870
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.15625
summary