Related gene-specific medical variations for Gene (Select 142678) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3294723	NM_080875.2(MIB2):c.11C>A (p.Ala4Glu)	LOC129929140, MIB2 (A4E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126111	NM_001170687.4(MIB2):c.-251C>T	LOC129929140, MIB2	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2517766	NM_080875.2(MIB2):c.38C>A (p.Ser13Tyr)	LOC129929140, MIB2 (S13Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491555	NM_001170687.4(MIB2):c.-252C>T	LOC129929140, MIB2	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2337746	NM_001170687.4(MIB2):c.-249A>G	LOC129929140, MIB2	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2271589	NM_001170687.4(MIB2):c.-179G>C	LOC129929140, MIB2	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2206699	NM_001170687.4(MIB2):c.-161T>C	LOC129929140, MIB2	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 791768	NM_080875.2(MIB2):c.10dup (p.Ala4Glyfs)	LOC129929140, MIB2	Duplication (frameshift variant)	not provided	GBenign
Select item 218832	NM_001170687.4(MIB2):c.-151C>A	LOC129929140, MIB2	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GLikely benign

ClinVar