Related gene-specific medical variations for Gene (Select 6736) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3242611	NC_000024.9:g.(?_2654792)_(2655895_?)del	SRY	Deletion	46,XY sex reversal 1	GPathogenic
Select item 3242237	NM_003140.3(SRY):c.-33T>A	LOC108178989, SRY	Single nucleotide variant (5 prime UTR variant)	46,XY disorder of sex development	GBenign
Select item 1339966	GRCh37/hg19 Yp11.31(chrY:2650140-2691749)x0	SRY	Copy number loss	not provided	GPathogenic
Select item 258964	NM_003140.3(SRY):c.*13A>G	SRY	Single nucleotide variant (3 prime UTR variant)	not specified	GLikely benign

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