List of variants in gene combination HCN4, LOC105370890, LOC126862173 reported by Fulgent Genetics, Fulgent Genetics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005477.3(HCN4):c.1115G>A (p.Arg372Gln)	rs748658688	0.00001
NM_005477.3(HCN4):c.1132C>T (p.Arg378Cys)	rs758468167	0.00001
NM_005477.3(HCN4):c.1026C>G (p.Phe342Leu)	rs2043017188
NM_005477.3(HCN4):c.1090G>C (p.Asp364His)	rs151004999
NM_005477.3(HCN4):c.1090G>T (p.Asp364Tyr)	rs151004999
NM_005477.3(HCN4):c.955G>A (p.Val319Met)	rs773269320

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