Related gene-specific medical variations for Gene (Select 6206) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3156181	NM_001016.4(RPS12):c.38A>G (p.Asp13Gly)	LOC129997182, RPS12 (D13G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395142	NM_001016.4(RPS12):c.71C>T (p.Thr24Ile)	LOC129997182, RPS12 (T24I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345854	NM_001016.4(RPS12):c.40G>A (p.Val14Ile)	LOC129997182, RPS12 (V14I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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