ClinVar Miner

List of variants reported as likely benign for autosomal recessive nonsyndromic hearing loss 66 by Labcorp Genetics (formerly Invitae), Labcorp

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 80
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_016356.5(DCDC2):c.1208G>A (p.Arg403His) rs139858268 0.00194
NM_016356.5(DCDC2):c.715T>G (p.Ser239Ala) rs144695853 0.00183
NM_016356.5(DCDC2):c.402G>A (p.Pro134=) rs142088541 0.00064
NM_016356.5(DCDC2):c.817C>T (p.Pro273Ser) rs146787541 0.00061
NM_016356.5(DCDC2):c.888A>G (p.Lys296=) rs41271773 0.00029
NM_016356.5(DCDC2):c.349-15C>T rs200146922 0.00025
NM_016356.5(DCDC2):c.222C>A (p.Ile74=) rs138670560 0.00023
NM_016356.5(DCDC2):c.923-12T>G rs200973005 0.00015
NM_016356.5(DCDC2):c.349-9C>G rs765613994 0.00013
NM_016356.5(DCDC2):c.1422C>T (p.Ala474=) rs146868469 0.00010
NM_016356.5(DCDC2):c.750T>G (p.Ser250=) rs372157851 0.00010
NM_016356.5(DCDC2):c.558-6C>T rs45520331 0.00009
NM_016356.5(DCDC2):c.68G>T (p.Arg23Leu) rs745333409 0.00008
NM_016356.5(DCDC2):c.705-4A>C rs774040286 0.00007
NM_016356.5(DCDC2):c.954G>A (p.Arg318=) rs140084657 0.00007
NM_016356.5(DCDC2):c.1221C>G (p.Gly407=) rs567036123 0.00006
NM_016356.5(DCDC2):c.366T>C (p.His122=) rs200657247 0.00005
NM_016356.5(DCDC2):c.1344A>G (p.Gln448=) rs368603558 0.00004
NM_016356.5(DCDC2):c.1147G>C (p.Asp383His) rs180988889 0.00003
NM_016356.5(DCDC2):c.1203T>A (p.Pro401=) rs143452599 0.00003
NM_016356.5(DCDC2):c.1224C>T (p.Thr408=) rs763861048 0.00003
NM_016356.5(DCDC2):c.1272A>G (p.Gln424=) rs755258271 0.00003
NM_016356.5(DCDC2):c.1359A>G (p.Pro453=) rs374448795 0.00003
NM_016356.5(DCDC2):c.1099T>A (p.Ser367Thr) rs538198742 0.00002
NM_016356.5(DCDC2):c.1326+9A>G rs752452396 0.00002
NM_016356.5(DCDC2):c.1327-15T>A rs1027558772 0.00002
NM_016356.5(DCDC2):c.1327-9T>C rs77929453 0.00002
NM_016356.5(DCDC2):c.759+17T>G rs751302256 0.00002
NM_016356.5(DCDC2):c.1024-16C>T rs754765133 0.00001
NM_016356.5(DCDC2):c.1275G>T (p.Leu425=) rs534996877 0.00001
NM_016356.5(DCDC2):c.293+20C>T rs772875683 0.00001
NM_016356.5(DCDC2):c.456A>G (p.Pro152=) rs764454438 0.00001
NM_016356.5(DCDC2):c.45C>A (p.Val15=) rs148029760 0.00001
NM_016356.5(DCDC2):c.471T>G (p.Leu157=) rs374456364 0.00001
NM_016356.5(DCDC2):c.557+14A>G rs775645058 0.00001
NM_016356.5(DCDC2):c.57G>T (p.Val19=) rs577487337 0.00001
NM_016356.5(DCDC2):c.732T>C (p.Ile244=) rs779146204 0.00001
NM_016356.5(DCDC2):c.922+19T>C rs555636841 0.00001
NM_016356.5(DCDC2):c.923-18G>A rs768651764 0.00001
NM_016356.5(DCDC2):c.923-8C>T rs1313039709 0.00001
NM_016356.5(DCDC2):c.93G>A (p.Gly31=) rs938050921 0.00001
NM_016356.5(DCDC2):c.999T>G (p.Thr333=) rs1561889345 0.00001
NM_016356.5(DCDC2):c.1023+11T>C rs2532262469
NM_016356.5(DCDC2):c.1023+14C>A rs1237059249
NM_016356.5(DCDC2):c.1024-5A>G
NM_016356.5(DCDC2):c.1024-9A>G
NM_016356.5(DCDC2):c.1026G>A (p.Arg342=)
NM_016356.5(DCDC2):c.1080A>G (p.Ala360=)
NM_016356.5(DCDC2):c.1134T>C (p.Gly378=)
NM_016356.5(DCDC2):c.1164C>T (p.Val388=) rs767129413
NM_016356.5(DCDC2):c.1224C>A (p.Thr408=) rs763861048
NM_016356.5(DCDC2):c.12C>T (p.Ser4=)
NM_016356.5(DCDC2):c.1326+19C>T
NM_016356.5(DCDC2):c.1332T>C (p.Asp444=)
NM_016356.5(DCDC2):c.144G>C (p.Leu48=) rs761682006
NM_016356.5(DCDC2):c.294-11T>A rs2532468828
NM_016356.5(DCDC2):c.349-8T>G rs2532402341
NM_016356.5(DCDC2):c.414G>A (p.Pro138=)
NM_016356.5(DCDC2):c.425+10A>T
NM_016356.5(DCDC2):c.425+11A>T rs1236878753
NM_016356.5(DCDC2):c.543C>A (p.Ser181Arg) rs141060456
NM_016356.5(DCDC2):c.543C>T (p.Ser181=) rs141060456
NM_016356.5(DCDC2):c.555C>T (p.His185=) rs2532401486
NM_016356.5(DCDC2):c.558-4A>G rs2532385482
NM_016356.5(DCDC2):c.558-5G>T rs748792618
NM_016356.5(DCDC2):c.687G>A (p.Thr229=)
NM_016356.5(DCDC2):c.696G>A (p.Arg232=) rs758802517
NM_016356.5(DCDC2):c.702T>C (p.Phe234=)
NM_016356.5(DCDC2):c.705-10G>T rs1554116524
NM_016356.5(DCDC2):c.705-11del rs758628136
NM_016356.5(DCDC2):c.759+9C>G
NM_016356.5(DCDC2):c.760-12T>C
NM_016356.5(DCDC2):c.760-7C>T rs2532366218
NM_016356.5(DCDC2):c.846C>T (p.Asp282=)
NM_016356.5(DCDC2):c.918T>C (p.Asn306=) rs1239033952
NM_016356.5(DCDC2):c.922+17T>C
NM_016356.5(DCDC2):c.923-10G>T rs745691985
NM_016356.5(DCDC2):c.923-12_923-9del rs761540134
NM_016356.5(DCDC2):c.923-5A>C
NM_016356.5(DCDC2):c.99C>T (p.Arg33=) rs755386397

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.