C3279791[trait identifier] AND "Center for Genomics, Ann and Robert H. - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 537959	NM_002471.4(MYH6):c.4438A>G (p.Ser1480Gly)	MYH6 (S1480G)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 14 +5 more	GUncertain significance
Select item 537942	NM_002471.4(MYH6):c.4264C>T (p.Arg1422Trp)	MYH6 (R1422W)	Single nucleotide variant (missense variant)	not provided +7 more	GUncertain significance
Select item 429310	NM_002471.4(MYH6):c.49C>T (p.Arg17Cys)	LOC114827851, MYH6 (R17C)	Single nucleotide variant (missense variant)	not provided +4 more	GUncertain significance

Format

Sort by

Choose Destination

ClinVar