Related gene-specific medical variations for Gene (Select 729515) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3327009	NM_018452.6(TMEM242):c.11C>A (p.Ala4Glu)	LOC129997541, TMEM242 (A4E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179258	NM_018452.6(TMEM242):c.16G>A (p.Ala6Thr)	LOC129997541, TMEM242 (A6T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488683	NM_018452.6(TMEM242):c.30G>C (p.Gln10His)	LOC129997541, TMEM242 (Q10H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488100	NM_018452.6(TMEM242):c.11C>G (p.Ala4Gly)	LOC129997541, TMEM242 (A4G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346547	NM_018452.6(TMEM242):c.32C>T (p.Pro11Leu)	LOC129997541, TMEM242 (P11L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315605	NM_018452.6(TMEM242):c.26G>A (p.Gly9Glu)	LOC129997541, TMEM242 (G9E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar