C3279693[trait identifier] AND "OMIM"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 29666	NM_181703.4(GJA5):c.685C>A (p.Leu229Met)	GJA5, LOC122128420 (L229M)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 11	GPathogenic
Select item 29665	NM_181703.4(GJA5):c.661C>A (p.Leu221Ile)	GJA5, LOC122128420 (L221I)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 11	GPathogenic
Select item 16998	NM_181703.4(GJA5):c.286G>T (p.Ala96Ser)	GJA5 (A96S)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 11 +2 more	GUncertain significance
Select item 29664	NM_181703.4(GJA5):c.253G>A (p.Val85Ile)	GJA5 (V85I)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 11	GPathogenic
Select item 126903	NM_181703.4(GJA5):c.223A>T (p.Ile75Phe)	GJA5 (I75F)	Single nucleotide variant (missense variant)	Atrial standstill 1 +1 more	GUncertain significance
Select item 29663	NM_181703.4(GJA5):c.145C>T (p.Gln49Ter)	GJA5 (Q49*)	Single nucleotide variant (nonsense)	Atrial fibrillation, familial, 11	GPathogenic

ClinVar