rs397515619
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs397515619(-;-) |
Make rs397515619(-;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 57232073 |
Gene | AURKC |
is a | snp |
is | mentioned by |
dbSNP | rs397515619 |
dbSNP (classic) | rs397515619 |
ClinGen | rs397515619 |
ebi | rs397515619 |
HLI | rs397515619 |
Exac | rs397515619 |
Gnomad | rs397515619 |
Varsome | rs397515619 |
LitVar | rs397515619 |
Map | rs397515619 |
PheGenI | rs397515619 |
Biobank | rs397515619 |
1000 genomes | rs397515619 |
hgdp | rs397515619 |
ensembl | rs397515619 |
geneview | rs397515619 |
scholar | rs397515619 |
rs397515619 | |
pharmgkb | rs397515619 |
gwascentral | rs397515619 |
openSNP | rs397515619 |
23andMe | rs397515619 |
SNPshot | rs397515619 |
SNPdbe | rs397515619 |
MSV3d | rs397515619 |
GWAS Ctlg | rs397515619 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397515619(-;-) |
Alt | rs397515619(-;-) |
Reference | Rs397515619(C;C) |
Significance | Pathogenic |
Disease | Infertility associated with multi-tailed spermatozoa and excessive DNA |
Variation | info |
Gene | AURKC |
CLNDBN | Infertility associated with multi-tailed spermatozoa and excessive DNA |
Reversed | 0 |
HGVS | NC_000019.9:g.57743441delC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000006686.4, |