List of variants in gene NUP155 reported as uncertain significance 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_153485.3(NUP155):c.1204G>A (p.Val402Met)	rs148814027	0.00044
NM_153485.3(NUP155):c.1348A>G (p.Met450Val)	rs374935918	0.00002
NM_153485.3(NUP155):c.3226C>T (p.Arg1076Cys)	rs376467373	0.00001
NM_153485.3(NUP155):c.1304A>G (p.Asn435Ser)
NM_153485.3(NUP155):c.3247C>T (p.Arg1083Trp)

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