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rs121908654

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908654(A;A)
Make rs121908654(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position57234985
GeneAURKC
is asnp
is mentioned by
dbSNPrs121908654
ebirs121908654
HLIrs121908654
Exacrs121908654
Varsomers121908654
Maprs121908654
PheGenIrs121908654
hapmaprs121908654
1000 genomesrs121908654
hgdprs121908654
ensemblrs121908654
gopubmedrs121908654
geneviewrs121908654
scholarrs121908654
googlers121908654
pharmgkbrs121908654
gwascentralrs121908654
openSNPrs121908654
23andMers121908654
23andMe allrs121908654
SNP Nexus

SNPshotrs121908654
SNPdbers121908654
MSV3drs121908654
GWAS Ctlgrs121908654
Max Magnitude0
OMIM603495
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908654(A;A)
Alt rs121908654(A;A)
Reference rs121908654(G;G)
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.57746353G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006687.3,