rs77559927
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs77559927(C;C) |
Make rs77559927(C;T) |
Make rs77559927(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 114179297 |
Gene | TDRD1 |
is a | snp |
is | mentioned by |
dbSNP | rs77559927 |
dbSNP (classic) | rs77559927 |
ClinGen | rs77559927 |
ebi | rs77559927 |
HLI | rs77559927 |
Exac | rs77559927 |
Gnomad | rs77559927 |
Varsome | rs77559927 |
LitVar | rs77559927 |
Map | rs77559927 |
PheGenI | rs77559927 |
Biobank | rs77559927 |
1000 genomes | rs77559927 |
hgdp | rs77559927 |
ensembl | rs77559927 |
geneview | rs77559927 |
scholar | rs77559927 |
rs77559927 | |
pharmgkb | rs77559927 |
gwascentral | rs77559927 |
openSNP | rs77559927 |
23andMe | rs77559927 |
SNPshot | rs77559927 |
SNPdbe | rs77559927 |
MSV3d | rs77559927 |
GWAS Ctlg | rs77559927 |
Max Magnitude | 0 |
[PMID 27233649] Association of a TDRD1 variant with spermatogenic failure susceptibility in the Han Chinese.