ClinVar Miner

List of variants reported as likely pathogenic for Autistic disorder of childhood onset

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 62
Download table as spreadsheet
HGVS dbSNP
NC_000001.11:g.(?_103175204)_(111410059_?)del
NC_000001.11:g.(?_204033173)_(208209798_?)del
NC_000001.11:g.(?_231740970)_(231949671_?)del
NC_000002.12:g.(?_235927172)_(236034017_?)del
NC_000003.12:g.(?_1133359)_(1192637_?)del
NC_000003.12:g.(?_1185337)_(1255844_?)del
NC_000003.12:g.(?_1204527)_(1310468_?)del
NC_000003.12:g.(?_1247669)_(1285156_?)del
NC_000003.12:g.(?_195939900)_(197632041_?)dup
NC_000003.12:g.(?_54166)_(2405982_?)dup
NC_000003.12:g.(?_60501297)_(60591815_?)del
NC_000004.12:g.(?_148159332)_(148473475_?)del
NC_000004.12:g.(?_185324779)_(188495308_?)dup
NC_000005.10:g.(?_114046360)_(118610426_?)dup
NC_000006.12:g.(?_162035873)_(162195188_?)del
NC_000006.12:g.(?_162036131)_(162191715_?)del
NC_000006.12:g.(?_162162293)_(162311859_?)del
NC_000006.12:g.(?_162184117)_(162211182_?)del
NC_000006.12:g.(?_162440726)_(162603304_?)del
NC_000007.14:g.(?_111777402)_(111865491_?)del
NC_000007.14:g.(?_146655407)_(146796363_?)del
NC_000007.14:g.(?_152454659)_(158705768_?)del
NC_000007.14:g.(?_158603240)_(159108319_?)dup
NC_000007.14:g.(?_52551984)_(56315037_?)dup
NC_000008.11:g.(?_3914469)_(4157437_?)del
NC_000008.11:g.(?_4410048)_(4458635_?)del
NC_000008.11:g.(?_52477663)_(52864628_?)dup
NC_000008.11:g.(?_52556598)_(52839580_?)dup
NC_000008.11:g.(?_9998540)_(10117911_?)del
NC_000009.12:g.(?_116611967)_(116683530_?)del
NC_000010.11:g.(?_53976705)_(54036062_?)del
NC_000011.10:g.(?_96535656)_(99184810_?)del
NC_000012.12:g.(?_28125337)_(28231096_?)del
NC_000013.11:g.(?_35011654)_(35113567_?)del
NC_000013.11:g.(?_35060502)_(35507109_?)del
NC_000015.10:g.(?_28465091)_(30182562_?)dup
NC_000016.10:g.(?_21928119)_(22428075_?)dup
NC_000016.10:g.(?_6759006)_(6789572_?)del
NC_000017.11:g.(?_14183541)_(15573247_?)del
NC_000017.11:g.(?_36357256)_(37995300_?)dup
NC_000018.10:g.(?_10000)_(1543845_?)del
NC_000019.10:g.(?_17607118)_(17624457_?)del
NC_000019.10:g.(?_7981357)_(10019383_?)dup
NC_000020.11:g.(?_14490624)_(14573076_?)del
NC_000020.11:g.(?_15307783)_(15453889_?)del
NC_000020.11:g.(?_25564868)_(25611357_?)del
NC_000020.11:g.(?_42303583)_(42488707_?)del
NC_000020.11:g.(?_42461895)_(42648116_?)del
NC_000020.11:g.(?_42526267)_(42726111_?)del
NC_000020.11:g.(?_42579501)_(42691367_?)del
NC_000021.9:g.(?_38981673)_(41568791_?)del
NC_000021.9:g.(?_43403441)_(46673937_?)dup
NC_000022.11:g.(?_21959229)_(22218520_?)del
NC_000023.11:g.(?_10000)_(22474705_?)dup
NC_000023.11:g.(?_31660226)_(31820401_?)del
NC_000023.11:g.(?_32345828)_(32377888_?)del
NC_000023.11:g.(?_44209146)_(46109507_?)del
NC_000023.11:g.(?_4692064)_(6048196_?)del
NC_000024.10:g.(?_1)_(57227415_?)dup
NM_000693.3(ALDH1A3):c.1514T>C (p.Ile505Thr) rs797046134
NM_001244810.1(FOXP1):c.1348+2T>C rs1057518999
NM_003593.2(FOXN1):c.146C>T (p.Ser49Leu) rs797046135

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.