Related gene-specific medical variations for Gene (Select 644192) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3347446	NM_001145155.2(NR2F2):c.37G>A (p.Gly13Ser)	NR2F2, NR2F2-AS1 (G13S)	Single nucleotide variant (missense variant)	NR2F2-related disorder	GUncertain significance
Select item 1291706	NM_001145155.2(NR2F2):c.43+114G>T	NR2F2, NR2F2-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 426710	NM_021005.3(NR2F2):c.-5753G>A	NR2F2, NR2F2-AS1	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance

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