ClinVar Miner

List of variants studied for Spermatogenic failure 11

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_152467.5(KLHL10):c.261C>T (p.Pro87=) rs1529933 0.75799
NM_152467.5(KLHL10):c.647A>C (p.Gln216Pro) rs116420871 0.00348
NM_152467.5(KLHL10):c.937G>A (p.Ala313Thr) rs370756367 0.00042
NM_152467.5(KLHL10):c.923T>C (p.Ile308Thr) rs377399919 0.00005
NM_152467.5(KLHL10):c.985C>T (p.Arg329Cys) rs782565913 0.00001
NM_152467.5(KLHL10):c.1014A>C (p.Lys338Asn) rs2544489279
NM_152467.5(KLHL10):c.1302+123_1302+126del rs534770865

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.