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rs10848911

From SNPedia

Orientationplus
Stabilizedplus
Make rs10848911(A;A)
Make rs10848911(A;G)
Make rs10848911(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position3705072
GeneEFCAB4B, LOC102723813
is asnp
is mentioned by
dbSNPrs10848911
ebirs10848911
HLIrs10848911
Exacrs10848911
Varsomers10848911
Maprs10848911
PheGenIrs10848911
hapmaprs10848911
1000 genomesrs10848911
hgdprs10848911
ensemblrs10848911
gopubmedrs10848911
geneviewrs10848911
scholarrs10848911
googlers10848911
pharmgkbrs10848911
gwascentralrs10848911
openSNPrs10848911
23andMers10848911
23andMe allrs10848911
SNP Nexus

SNPshotrs10848911
SNPdbers10848911
MSV3drs10848911
GWAS Ctlgrs10848911
GMAF0.2057
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 0.000004
Odds Ratio NR NR


GET Evidence
rs10848911
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary