ClinVar Miner

List of variants in gene MCFD2 reported as uncertain significance for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
Download table as spreadsheet
HGVS dbSNP
NM_001171506.2(MCFD2):c.*2780_*2781del rs886056109
NM_001171506.2(MCFD2):c.-184_-183del rs886056120
NM_001171506.2(MCFD2):c.-184del rs886056122
NM_001171506.2(MCFD2):c.-185_-183del rs886056121
NM_001171506.2(MCFD2):c.-189_-186del rs886056123
NM_001171506.2(MCFD2):c.-189del rs886056124
NM_139279.5(MCFD2):c.*1043G>A rs114662283
NM_139279.5(MCFD2):c.*1111G>C rs181922575
NM_139279.5(MCFD2):c.*1158C>A rs886056113
NM_139279.5(MCFD2):c.*1289T>C rs527427772
NM_139279.5(MCFD2):c.*1314C>T rs150644996
NM_139279.5(MCFD2):c.*1354G>T rs886056112
NM_139279.5(MCFD2):c.*1415C>T rs147096932
NM_139279.5(MCFD2):c.*1724C>T rs115137793
NM_139279.5(MCFD2):c.*173G>T rs886056116
NM_139279.5(MCFD2):c.*1788C>T rs115043642
NM_139279.5(MCFD2):c.*1875T>C rs552695942
NM_139279.5(MCFD2):c.*1995G>A rs183896754
NM_139279.5(MCFD2):c.*2017C>T rs886056111
NM_139279.5(MCFD2):c.*2121G>A rs187335799
NM_139279.5(MCFD2):c.*2141G>C rs546151221
NM_139279.5(MCFD2):c.*2169G>A rs79487300
NM_139279.5(MCFD2):c.*2336A>C rs144118640
NM_139279.5(MCFD2):c.*2565A>G rs886056110
NM_139279.5(MCFD2):c.*2789G>C rs886056108
NM_139279.5(MCFD2):c.*2848C>T rs142254354
NM_139279.5(MCFD2):c.*3014G>A rs886056107
NM_139279.5(MCFD2):c.*3072_*3073insGG rs559484016
NM_139279.5(MCFD2):c.*3099G>A rs886056106
NM_139279.5(MCFD2):c.*3100C>G rs13424086
NM_139279.5(MCFD2):c.*311G>A rs886056115
NM_139279.5(MCFD2):c.*3293A>C rs763634945
NM_139279.5(MCFD2):c.*3354A>G rs886056105
NM_139279.5(MCFD2):c.*428G>A rs781195000
NM_139279.5(MCFD2):c.*517C>G rs761766519
NM_139279.5(MCFD2):c.*557G>A rs185756640
NM_139279.5(MCFD2):c.*569G>A rs149363149
NM_139279.5(MCFD2):c.*62T>G rs886056117
NM_139279.5(MCFD2):c.*64T>C rs754447509
NM_139279.5(MCFD2):c.*73A>G rs71423925
NM_139279.5(MCFD2):c.*84T>C rs182576601
NM_139279.5(MCFD2):c.*892G>A rs886056114
NM_139279.5(MCFD2):c.*912C>T rs189018618
NM_139279.5(MCFD2):c.-34C>A rs886056119
NM_139279.5(MCFD2):c.-7+11T>A rs201752014
NM_139279.5(MCFD2):c.-95C>G rs886056125
NM_139279.5(MCFD2):c.106C>G (p.Pro36Ala) rs756021929
NM_139279.5(MCFD2):c.236T>C (p.Met79Thr) rs886056118
NM_139279.5(MCFD2):c.310-11G>C rs144139062
NM_139279.5(MCFD2):c.416C>T (p.Ala139Val) rs80294301

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.