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rs397515484

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515484(A;G)
Make rs397515484(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position57233458
GeneAURKC
is asnp
is mentioned by
dbSNPrs397515484
ebirs397515484
HLIrs397515484
Exacrs397515484
Varsomers397515484
Maprs397515484
PheGenIrs397515484
hapmaprs397515484
1000 genomesrs397515484
hgdprs397515484
ensemblrs397515484
gopubmedrs397515484
geneviewrs397515484
scholarrs397515484
googlers397515484
pharmgkbrs397515484
gwascentralrs397515484
openSNPrs397515484
23andMers397515484
23andMe allrs397515484
SNP Nexus

SNPshotrs397515484
SNPdbers397515484
MSV3drs397515484
GWAS Ctlgrs397515484
Max Magnitude0
ClinVar
Risk rs397515484(G;G)
Alt rs397515484(G;G)
Reference rs397515484(A;A)
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.57744826A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000056325.2,