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rs397515619

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515619(-;-)
Make rs397515619(-;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position57232073
GeneAURKC
is asnp
is mentioned by
dbSNPrs397515619
ebirs397515619
HLIrs397515619
Exacrs397515619
Varsomers397515619
Maprs397515619
PheGenIrs397515619
hapmaprs397515619
1000 genomesrs397515619
hgdprs397515619
ensemblrs397515619
gopubmedrs397515619
geneviewrs397515619
scholarrs397515619
googlers397515619
pharmgkbrs397515619
gwascentralrs397515619
openSNPrs397515619
23andMers397515619
23andMe allrs397515619
SNP Nexus

SNPshotrs397515619
SNPdbers397515619
MSV3drs397515619
GWAS Ctlgrs397515619
Max Magnitude0
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 RCV000006686.3,