ClinVar Miner

List of variants studied for intellectual disability, autosomal dominant 1 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

Included ClinVar conditions (1):

Intellectual disability, autosomal dominant 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001378120.1(MBD5):c.1017TCC[1] (p.Pro342del)	rs1388983985
NM_001378120.1(MBD5):c.278A>G (p.Asp93Gly)
NM_001378120.1(MBD5):c.3800C>T (p.Thr1267Ile)	rs1681444814
NM_001378120.1(MBD5):c.4031C>T (p.Thr1344Ile)

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