List of variants in gene combination IL17RC, LOC129936144 studied for not specified

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_153460.4(IL17RC):c.2152G>A (p.Asp718Asn)	rs755919625	0.00008
NM_153460.4(IL17RC):c.2137G>A (p.Gly713Arg)	rs781031468	0.00004
NM_153460.4(IL17RC):c.2144G>A (p.Gly715Glu)	rs752392891	0.00003
NM_153460.4(IL17RC):c.2057G>A (p.Arg686Gln)	rs771035296
NM_153460.4(IL17RC):c.2059G>T (p.Ala687Ser)
NM_153460.4(IL17RC):c.2107G>A (p.Ala703Thr)	rs980705815
NM_153460.4(IL17RC):c.2147C>T (p.Ala716Val)	rs867817700
NM_153460.4(IL17RC):c.2155G>C (p.Gly719Arg)	rs777636561

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