C4225308[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1165169	NM_021619.3(PRDM12):c.648C>T (p.Pro216=)	PRDM12	Single nucleotide variant (synonymous variant)	Congenital insensitivity to pain-hypohidrosis syndrome +1 more	GBenign
Select item 1225621	NM_021619.3(PRDM12):c.682+38A>G	PRDM12	Single nucleotide variant (intron variant)	Congenital insensitivity to pain-hypohidrosis syndrome +1 more	GBenign