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rs116420871

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs116420871(A;C)
Make rs116420871(C;C)
ReferenceGRCh38 38.1/142
Chromosome17
Position41842275
GeneKLHL10
is asnp
is mentioned by
dbSNPrs116420871
ebirs116420871
HLIrs116420871
Exacrs116420871
Varsomers116420871
Maprs116420871
PheGenIrs116420871
hapmaprs116420871
1000 genomesrs116420871
hgdprs116420871
ensemblrs116420871
gopubmedrs116420871
geneviewrs116420871
scholarrs116420871
googlers116420871
pharmgkbrs116420871
gwascentralrs116420871
openSNPrs116420871
23andMers116420871
23andMe allrs116420871
SNP Nexus

SNPshotrs116420871
SNPdbers116420871
MSV3drs116420871
GWAS Ctlgrs116420871
Max Magnitude0
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
CLNACC RCV000033135.2,