List of variants reported as likely pathogenic for autism, susceptiblity to by Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001170629.2(CHD8):c.1601+5G>A	rs2139531134
NM_001170629.2(CHD8):c.3299T>C (p.Leu1100Pro)
NM_001170629.2(CHD8):c.4611del (p.Lys1537_Val1538insTer)	rs1555314317
NM_006593.4(TBR1):c.691A>G (p.Arg231Gly)
NM_012309.5(SHANK2):c.3953_3958delinsGC (p.Thr1318fs)

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