rs864309485
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs864309485(G;G) |
Make rs864309485(G;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 8 |
Position | 30846888 |
Gene | TEX15 |
is a | snp |
is | mentioned by |
dbSNP | rs864309485 |
dbSNP (classic) | rs864309485 |
ClinGen | rs864309485 |
ebi | rs864309485 |
HLI | rs864309485 |
Exac | rs864309485 |
Gnomad | rs864309485 |
Varsome | rs864309485 |
LitVar | rs864309485 |
Map | rs864309485 |
PheGenI | rs864309485 |
Biobank | rs864309485 |
1000 genomes | rs864309485 |
hgdp | rs864309485 |
ensembl | rs864309485 |
geneview | rs864309485 |
scholar | rs864309485 |
rs864309485 | |
pharmgkb | rs864309485 |
gwascentral | rs864309485 |
openSNP | rs864309485 |
23andMe | rs864309485 |
SNPshot | rs864309485 |
SNPdbe | rs864309485 |
MSV3d | rs864309485 |
GWAS Ctlg | rs864309485 |
Max Magnitude | 0 |
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, |