List of variants reported as likely benign for Syndromic intellectual disability by Illumina Laboratory Services, Illumina

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

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_001377265.1(MAPT):c.*1047C>T	rs113815715	0.02477
NM_001377265.1(MAPT):c.*2810G>A	rs2158256	0.02237
NM_001377265.1(MAPT):c.*2167G>A	rs16940802	0.01564
NM_001377265.1(MAPT):c.*2991C>T	rs141337757	0.01116
NM_001377265.1(MAPT):c.*3435T>C	rs186977284	0.00544
NM_001377265.1(MAPT):c.*2956T>C	rs181844055	0.00514
NM_015443.4(KANSL1):c.*1196T>G	rs137970866	0.00488
NM_015443.4(KANSL1):c.*1027C>G	rs11870461	0.00390
NM_015443.4(KANSL1):c.34_37del	rs373668834	0.00257
NM_001377265.1(MAPT):c.*3377G>C	rs540687358	0.00235
NM_001377265.1(MAPT):c.*1721C>T	rs186042163	0.00190
NM_015443.4(KANSL1):c.*217C>T	rs140200874	0.00136
NM_001377265.1(MAPT):c.*3570T>C	rs567899904	0.00098
NM_001377265.1(MAPT):c.*1465C>T	rs189665411	0.00039
NM_015443.4(KANSL1):c.*626T>C	rs533537317	0.00022
NM_001377265.1(MAPT):c.*3810G>A	rs140613804	0.00007
NM_001377265.1(MAPT):c.*3133A>G	rs191084195	0.00002
NM_001377265.1(MAPT):c.*1670C>T	rs535931288	0.00001
NM_001377265.1(MAPT):c.*4154T>C	rs377535401	0.00001
NM_001377265.1(MAPT):c.*1039C>T	rs568260584
NM_001377265.1(MAPT):c.*1404T>C	rs530779128
NM_015443.4(KANSL1):c.*1028T>C	rs375427074
NM_015443.4(KANSL1):c.*388G>T	rs367998611
NM_015443.4(KANSL1):c.-90+55_-90+57del	rs534448299

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