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rs864309485

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864309485(G;G)
Make rs864309485(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position30846888
GeneTEX15
is asnp
is mentioned by
dbSNPrs864309485
ebirs864309485
HLIrs864309485
Exacrs864309485
Varsomers864309485
Maprs864309485
PheGenIrs864309485
hapmaprs864309485
1000 genomesrs864309485
hgdprs864309485
ensemblrs864309485
gopubmedrs864309485
geneviewrs864309485
scholarrs864309485
googlers864309485
pharmgkbrs864309485
gwascentralrs864309485
openSNPrs864309485
23andMers864309485
23andMe allrs864309485
SNP Nexus

SNPshotrs864309485
SNPdbers864309485
MSV3drs864309485
GWAS Ctlgrs864309485
Max Magnitude0
ClinVar
Risk rs864309485(G;G)
Alt rs864309485(G;G)
Reference rs864309485(T;T)
Significance Pathogenic
Disease Oligosynaptic infertility
Variation info
Gene TEX15
CLNDBN Oligosynaptic infertility
Reversed 1
HGVS NC_000008.10:g.30704404A>C
CLNSRC
CLNACC RCV000202575.1,