rs116420871
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs116420871(A;C) |
Make rs116420871(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 41842275 |
Gene | KLHL10 |
is a | snp |
is | mentioned by |
dbSNP | rs116420871 |
dbSNP (classic) | rs116420871 |
ClinGen | rs116420871 |
ebi | rs116420871 |
HLI | rs116420871 |
Exac | rs116420871 |
Gnomad | rs116420871 |
Varsome | rs116420871 |
LitVar | rs116420871 |
Map | rs116420871 |
PheGenI | rs116420871 |
Biobank | rs116420871 |
1000 genomes | rs116420871 |
hgdp | rs116420871 |
ensembl | rs116420871 |
geneview | rs116420871 |
scholar | rs116420871 |
rs116420871 | |
pharmgkb | rs116420871 |
gwascentral | rs116420871 |
openSNP | rs116420871 |
23andMe | rs116420871 |
SNPshot | rs116420871 |
SNPdbe | rs116420871 |
MSV3d | rs116420871 |
GWAS Ctlg | rs116420871 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs116420871(C;C) |
Alt | rs116420871(C;C) |
Reference | Rs116420871(A;A) |
Significance | Pathogenic |
Disease | Spermatogenic failure 11 |
Variation | info |
Gene | KLHL10 |
CLNDBN | Spermatogenic failure 11 |
Reversed | 0 |
HGVS | NC_000017.10:g.39998527A>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000033135.2, |