Related gene-specific medical variations for Gene (Select 79957) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2461066	NM_198406.3(PAQR6):c.407C>T (p.Ala136Val)	LOC129931613, PAQR6 (A30V +3 more)	Single nucleotide variant (non-coding transcript variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2456984	NM_198406.3(PAQR6):c.424T>A (p.Ser142Thr)	LOC129931613, PAQR6 (S36T +2 more)	Single nucleotide variant (missense variant +3 more)	Inborn genetic diseases	GUncertain significance