List of variants in gene IL17RD, LOC126806689 studied for Kallmann syndrome

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_017563.5(IL17RD):c.1531T>C (p.Leu511=)	rs2291462	0.78630
NM_017563.5(IL17RD):c.1373C>G (p.Ala458Gly)	rs867131722	0.00001
NM_017563.5(IL17RD):c.1645A>G (p.Met549Val)
NM_017563.5(IL17RD):c.1705C>T (p.Pro569Ser)
NM_017563.5(IL17RD):c.1992C>G (p.Ile664Met)
NM_017563.5(IL17RD):c.2101G>A (p.Gly701Ser)

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