C2751812[trait identifier] AND "Clinical Genetics DNA and cytogenetics - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 196565	NM_032273.4(TMEM126A):c.154A>G (p.Ser52Gly)	TMEM126A (S52G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +3 more	GBenign/Likely benign
Select item 137670	NM_032273.4(TMEM126A):c.191G>A (p.Arg64His)	TMEM126A (R64H)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +2 more	GBenign/Likely benign