"Genetic Services Laboratory, University of Chicago"[submitter] AND "Z - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 414004	NM_012082.4(ZFPM2):c.965-9TC[2]	ZFPM2-AS1, ZFPM2	Microsatellite (intron variant)	46,XY sex reversal 9 +1 more	GBenign
Select item 695890	NM_012082.4(ZFPM2):c.1015G>A (p.Val339Ile)	ZFPM2, ZFPM2-AS1 (V286I +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign
Select item 1150026	NM_012082.4(ZFPM2):c.1160C>G (p.Pro387Arg)	ZFPM2, ZFPM2-AS1 (P255R +2 more)	Single nucleotide variant (missense variant)	46,XY sex reversal 9 +2 more	GConflicting classifications of pathogenicity
Select item 544225	NM_012082.4(ZFPM2):c.1276G>A (p.Ala426Thr)	ZFPM2, ZFPM2-AS1 (A426T +2 more)	Single nucleotide variant (missense variant)	46,XY sex reversal 9 +2 more	GBenign/Likely benign
Select item 39518	NM_012082.4(ZFPM2):c.1632G>A (p.Met544Ile)	ZFPM2, ZFPM2-AS1 (M544I +2 more)	Single nucleotide variant (missense variant)	ZFPM2-related condition +3 more	GConflicting classifications of pathogenicity
Select item 1338377	NM_012082.4(ZFPM2):c.1975_1977del (p.Asn659del)	ZFPM2, ZFPM2-AS1 (N527del +2 more)	Deletion (inframe_deletion)	not specified	GUncertain significance
Select item 414003	NM_012082.4(ZFPM2):c.2287G>A (p.Val763Ile)	LOC126860469, ZFPM2 +1 more (V763I +2 more)	Single nucleotide variant (missense variant)	46,XY sex reversal 9 +2 more	GBenign/Likely benign
Select item 1167133	NM_012082.4(ZFPM2):c.2430A>T (p.Pro810=)	LOC126860469, ZFPM2 +1 more	Single nucleotide variant (synonymous variant)	46,XY sex reversal 9 +1 more	GBenign/Likely benign
Select item 697278	NM_012082.4(ZFPM2):c.2490A>T (p.Ile830=)	LOC126860469, ZFPM2 +1 more	Single nucleotide variant (synonymous variant)	ZFPM2-related condition +2 more	GBenign/Likely benign
Select item 544227	NM_012082.4(ZFPM2):c.2501A>G (p.Lys834Arg)	LOC126860469, ZFPM2 +1 more (K834R +2 more)	Single nucleotide variant (missense variant)	ZFPM2-related condition +2 more	GBenign/Likely benign
Select item 240843	NM_012082.4(ZFPM2):c.2665C>G (p.Gln889Glu)	LOC126860469, ZFPM2 +1 more (Q889E +2 more)	Single nucleotide variant (missense variant)	46,XY sex reversal 9 +1 more	GBenign