C3150998[trait identifier] AND "Clinical Genetics DNA and cytogenetics - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 128388	NM_018075.5(ANO10):c.1682C>T (p.Thr561Met)	ANO10 (T561M +4 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 128387	NM_018075.5(ANO10):c.1385G>A (p.Arg462Gln)	ANO10 (R462Q +3 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 260993	NM_018075.5(ANO10):c.1293+9A>G	ANO10	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 128386	NM_018075.5(ANO10):c.1066A>G (p.Ser356Gly)	ANO10 (S356G +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 345189	NM_018075.5(ANO10):c.980A>G (p.Tyr327Cys)	ANO10 (Y327C +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 901814	NM_018075.5(ANO10):c.788G>A (p.Arg263His)	ANO10 (R152H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GBenign/Likely benign

ClinVar