"SLC10A7-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 713617	NM_001029998.6(SLC10A7):c.928G>A (p.Ala310Thr)	SLC10A7 (A310T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1549029	NM_001029998.6(SLC10A7):c.711A>G (p.Ile237Met)	SLC10A7 (I224M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2198698	NM_001029998.6(SLC10A7):c.613A>G (p.Ile205Val)	SLC10A7 (I192V +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 2052257	NM_001029998.6(SLC10A7):c.442G>A (p.Val148Ile)	SLC10A7 (V135I +1 more)	Single nucleotide variant (missense variant +1 more)	SLC10A7-related disorder +1 more	GLikely benign
Select item 1634711	NM_001029998.6(SLC10A7):c.162T>C (p.Ser54=)	SLC10A7	Single nucleotide variant (synonymous variant +1 more)	SLC10A7-related disorder +1 more	GBenign
Select item 1544510	NM_001029998.6(SLC10A7):c.18A>C (p.Arg6Ser)	SLC10A7 (R6S)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign

ClinVar