ClinVar Miner

List of variants in gene combination MYH2, MYHAS reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 57
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_017534.6(MYH2):c.-20-217G>A rs7215791 0.87767
NM_017534.6(MYH2):c.5673+64G>A rs7223755 0.51988
NM_017534.6(MYH2):c.5673+141T>C rs7224268 0.51966
NM_017534.6(MYH2):c.324A>G (p.Glu108=) rs12600539 0.42634
NM_017534.6(MYH2):c.1148-98A>G rs2277653 0.40624
NM_017534.6(MYH2):c.3745-84T>C rs12952334 0.40478
NM_017534.6(MYH2):c.3745-154C>A rs9899992 0.40054
NM_017534.6(MYH2):c.3745-274T>C rs12952878 0.39972
NM_017534.6(MYH2):c.904+10G>A rs719277 0.39768
NM_017534.6(MYH2):c.2697+25A>G rs3744565 0.39755
NM_017534.6(MYH2):c.349-177G>A rs11078851 0.39356
NM_017534.6(MYH2):c.505+311T>C rs62060666 0.38931
NM_017534.6(MYH2):c.3263+15A>G rs2277651 0.34231
NM_017534.6(MYH2):c.5674-168A>G rs71360268 0.07456
NM_017534.6(MYH2):c.3872-310C>T rs35941696 0.06310
NM_017534.6(MYH2):c.5673+191T>A rs12937587 0.06305
NM_017534.6(MYH2):c.505+302G>T rs75020870 0.06269
NM_017534.6(MYH2):c.2180+210T>C rs34681441 0.06221
NM_017534.6(MYH2):c.3117+32C>T rs2277652 0.06211
NM_017534.6(MYH2):c.1975-9G>A rs3744566 0.06015
NM_017534.6(MYH2):c.1897+170G>A rs12953213 0.05747
NM_017534.6(MYH2):c.905-212C>T rs71360273 0.05676
NM_017534.6(MYH2):c.2181-51C>T rs71360269 0.05601
NM_017534.6(MYH2):c.5175+217G>A rs12947406 0.05541
NM_017534.6(MYH2):c.1974+77T>C rs3744568 0.05344
NM_017534.6(MYH2):c.2442-206T>C rs79807358 0.05211
NM_017534.6(MYH2):c.905-74C>T rs35760495 0.05153
NM_017534.6(MYH2):c.1975-47A>G rs3744567 0.05149
NM_017534.6(MYH2):c.1974+163T>C rs71360272 0.05140
NM_017534.6(MYH2):c.4187+121G>A rs12950718 0.05053
NM_017534.6(MYH2):c.4187+275C>T rs34499338 0.04719
NM_017534.6(MYH2):c.2181-80A>T rs71360270 0.04294
NM_017534.6(MYH2):c.4188-68G>A rs36082989 0.04289
NM_017534.6(MYH2):c.5176-26T>A rs117415453 0.04100
NM_017534.6(MYH2):c.1416+74A>T rs73974759 0.01630
NM_017534.6(MYH2):c.2967A>G (p.Ala989=) rs113190032 0.01110
NM_017534.6(MYH2):c.183G>A (p.Thr61=) rs142539913 0.00745
NM_017534.6(MYH2):c.2382C>A (p.Thr794=) rs76400103 0.00548
NM_017534.6(MYH2):c.4242C>T (p.Asn1414=) rs146615128 0.00548
NM_017534.6(MYH2):c.2908G>A (p.Val970Ile) rs143872329 0.00456
NM_017534.6(MYH2):c.3181C>G (p.Leu1061Val) rs142586585 0.00225
NM_017534.6(MYH2):c.2414T>C (p.Val805Ala) rs200662973 0.00034
NM_017534.6(MYH2):c.3582A>G (p.Thr1194=) rs200505060 0.00034
NM_017534.6(MYH2):c.-20-260A>T rs62060669
NM_017534.6(MYH2):c.1008+222_1008+223dup rs56139789
NM_017534.6(MYH2):c.1008+222_1008+224dup rs56139789
NM_017534.6(MYH2):c.1008+233_1008+234del rs56139789
NM_017534.6(MYH2):c.1008+234del rs56139789
NM_017534.6(MYH2):c.2181-256C>G rs12938380
NM_017534.6(MYH2):c.2442-126dup rs11379780
NM_017534.6(MYH2):c.3744+124dup rs11372676
NM_017534.6(MYH2):c.3745-188_3745-185dup rs71365770
NM_017534.6(MYH2):c.399T>A (p.Pro133=) rs11078850
NM_017534.6(MYH2):c.505+313T>C rs62060665
NM_017534.6(MYH2):c.5674-168AT[11] rs3051834
NM_017534.6(MYH2):c.5674-168AT[12] rs3051834
NM_017534.6(MYH2):c.905-154C>A rs11652345

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.