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rs370756367

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs370756367(A;A)
Make rs370756367(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position41845378
GeneKLHL10
is asnp
is mentioned by
dbSNPrs370756367
ebirs370756367
HLIrs370756367
Exacrs370756367
Varsomers370756367
Maprs370756367
PheGenIrs370756367
hapmaprs370756367
1000 genomesrs370756367
hgdprs370756367
ensemblrs370756367
gopubmedrs370756367
geneviewrs370756367
scholarrs370756367
googlers370756367
pharmgkbrs370756367
gwascentralrs370756367
openSNPrs370756367
23andMers370756367
23andMe allrs370756367
SNP Nexus

SNPshotrs370756367
SNPdbers370756367
MSV3drs370756367
GWAS Ctlgrs370756367
Max Magnitude0
ClinVar
Risk rs370756367(A;A)
Alt rs370756367(A;A)
Reference rs370756367(G;G)
Significance Pathogenic
Disease Spermatogenic failure 11
Variation info
Gene KLHL10
CLNDBN Spermatogenic failure 11
Reversed 0
HGVS NC_000017.10:g.40001630G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000033136.2,