List of variants in gene C2CD3, LOC126861262 studied for Inborn genetic diseases

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001286577.2(C2CD3):c.5726T>C (p.Leu1909Pro)	rs138354490	0.00014
NM_001286577.2(C2CD3):c.5728C>G (p.Pro1910Ala)	rs150116588	0.00012
NM_001286577.2(C2CD3):c.5672G>A (p.Ser1891Asn)	rs1952808152	0.00001
NM_001286577.2(C2CD3):c.5710C>G (p.Leu1904Val)	rs370958538	0.00001
NM_001286577.2(C2CD3):c.5815C>T (p.Pro1939Ser)	rs774993707	0.00001
NM_001286577.2(C2CD3):c.5737C>T (p.Pro1913Ser)
NM_001286577.2(C2CD3):c.5864T>C (p.Val1955Ala)	rs1365676217

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