List of variants in gene AHDC1 reported as likely benign for syndromic intellectual disability

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001371928.1(AHDC1):c.2634C>T (p.Ala878=)	rs60039430	0.01134
NM_001371928.1(AHDC1):c.811C>G (p.Pro271Ala)	rs200660997	0.00281
NM_001371928.1(AHDC1):c.4585C>T (p.Arg1529Cys)	rs200178921	0.00032
NM_001371928.1(AHDC1):c.1172A>G (p.Lys391Arg)
NM_001371928.1(AHDC1):c.3254CCT[6] (p.Ser1091del)	rs530256606
NM_001371928.1(AHDC1):c.3254CCT[8] (p.Ser1091dup)	rs530256606
NM_001371928.1(AHDC1):c.337A>T (p.Asn113Tyr)	rs1135401946
NM_001371928.1(AHDC1):c.3547C>G (p.Arg1183Gly)
NM_001371928.1(AHDC1):c.640C>T (p.His214Tyr)

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