List of variants in gene combination GJA5, LOC122128420 reported as likely benign for atrial fibrillation

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_181703.4(GJA5):c.798C>T (p.Asp266=)	rs116155008	0.00014
NM_181703.4(GJA5):c.567C>G (p.Pro189=)	rs2148959089
NM_181703.4(GJA5):c.576C>T (p.His192=)
NM_181703.4(GJA5):c.591C>T (p.Tyr197=)
NM_181703.4(GJA5):c.618C>G (p.Val206=)	rs2148959048
NM_181703.4(GJA5):c.645T>A (p.Ala215=)
NM_181703.4(GJA5):c.685C>T (p.Leu229=)
NM_181703.4(GJA5):c.738T>C (p.Ala246=)	rs2148958978
NM_181703.4(GJA5):c.756C>A (p.Gly252=)
NM_181703.4(GJA5):c.765G>C (p.Val255=)	rs2148958937
NM_181703.4(GJA5):c.780C>T (p.Ser260=)	rs1663834363
NM_181703.4(GJA5):c.789A>G (p.Pro263=)
NM_181703.4(GJA5):c.795C>T (p.Pro265=)
NM_181703.4(GJA5):c.813G>A (p.Leu271=)	rs2148958892
NM_181703.4(GJA5):c.843T>C (p.Asn281=)

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