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rs1399645

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1399645(A;A)
Make rs1399645(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position139390262
is asnp
is mentioned by
dbSNPrs1399645
ebirs1399645
HLIrs1399645
Exacrs1399645
Varsomers1399645
Maprs1399645
PheGenIrs1399645
hapmaprs1399645
1000 genomesrs1399645
hgdprs1399645
ensemblrs1399645
gopubmedrs1399645
geneviewrs1399645
scholarrs1399645
googlers1399645
pharmgkbrs1399645
gwascentralrs1399645
openSNPrs1399645
23andMers1399645
23andMe allrs1399645
SNP Nexus

SNPshotrs1399645
SNPdbers1399645
MSV3drs1399645
GWAS Ctlgrs1399645
GMAF0.1391
Max Magnitude0
? (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 9E-7
Odds Ratio NR NR


GET Evidence
rs1399645
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.117188
summary