List of variants in gene KLHL10 studied for Spermatogenic failure 11

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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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

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