Related gene-specific medical variations for Gene (Select 3270) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 35487	NM_017636.4(TRPM4):c.1294G>A (p.Ala432Thr)	HRC, TRPM4 (A432T +3 more)	Single nucleotide variant (missense variant +1 more)	Progressive familial heart block type IB +4 more	GConflicting classifications of pathogenicity
Select item 35486	NM_017636.4(TRPM4):c.1744G>A (p.Gly582Ser)	HRC, TRPM4 (G582S +4 more)	Single nucleotide variant (missense variant)	Progressive familial heart block type IB +4 more	GConflicting classifications of pathogenicity