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Items: 2

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
ChrX:10535245
GRCh38:
ChrX:10567205
MID1Opitz-Frias syndromePathogenic
(Oct 12, 2000)
no assertion criteria provided
2.
GRCh37:
ChrX:10417535
GRCh38:
ChrX:10449495
MID1Opitz-Frias syndromePathogenic
(Oct 12, 2000)
no assertion criteria provided
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