ClinVar Miner

List of variants in gene MCFD2 studied for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 78
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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_001171506.2(MCFD2):c.-198_-190del rs372282781
NM_001171506.2(MCFD2):c.103del (p.Gln35fs) rs1253799389
NM_001171506.2(MCFD2):c.149+5G>A rs387906286
NM_001171506.2(MCFD2):c.249del (p.Asp83fs) rs1294221028
NM_001171506.2(MCFD2):c.265_272del (p.Asp89fs) rs1558461545
NM_001171506.2(MCFD2):c.375_376GA[4] (p.Asp127fs)
NM_139279.5(MCFD2):c.*1010G>T rs138758588
NM_139279.5(MCFD2):c.*1042C>T rs111603188
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.*1267G>T rs7596245
NM_139279.5(MCFD2):c.*1289T>C rs527427772
NM_139279.5(MCFD2):c.*1314C>T rs150644996
NM_139279.5(MCFD2):c.*133A>T rs75416242
NM_139279.5(MCFD2):c.*1346G>T rs111535939
NM_139279.5(MCFD2):c.*1354G>T rs886056112
NM_139279.5(MCFD2):c.*1415C>T rs147096932
NM_139279.5(MCFD2):c.*1525C>G rs7596198
NM_139279.5(MCFD2):c.*1677T>G rs28770495
NM_139279.5(MCFD2):c.*1724C>T rs115137793
NM_139279.5(MCFD2):c.*173G>T rs886056116
NM_139279.5(MCFD2):c.*1752T>C rs6544935
NM_139279.5(MCFD2):c.*1788C>T rs115043642
NM_139279.5(MCFD2):c.*1875T>C rs552695942
NM_139279.5(MCFD2):c.*1908G>C rs6743994
NM_139279.5(MCFD2):c.*1924T>C rs6715391
NM_139279.5(MCFD2):c.*1995G>A rs183896754
NM_139279.5(MCFD2):c.*2017C>T rs886056111
NM_139279.5(MCFD2):c.*2075C>T rs6743966
NM_139279.5(MCFD2):c.*2121G>A rs187335799
NM_139279.5(MCFD2):c.*2141G>C rs546151221
NM_139279.5(MCFD2):c.*2163A>G rs140937815
NM_139279.5(MCFD2):c.*2169G>A rs79487300
NM_139279.5(MCFD2):c.*2336A>C rs144118640
NM_139279.5(MCFD2):c.*2454C>A rs1051317
NM_139279.5(MCFD2):c.*2565A>G rs886056110
NM_139279.5(MCFD2):c.*2658C>T rs17035887
NM_139279.5(MCFD2):c.*2675C>G rs17035884
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.*3318T>C rs8861
NM_139279.5(MCFD2):c.*3354A>G rs886056105
NM_139279.5(MCFD2):c.*428G>A rs781195000
NM_139279.5(MCFD2):c.*498A>G rs144674773
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.*693G>C rs28516550
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.241G>T (p.Asp81Tyr) rs78289603
NM_139279.5(MCFD2):c.309+1G>A rs387906287
NM_139279.5(MCFD2):c.310-11G>C rs144139062
NM_139279.5(MCFD2):c.387C>G (p.Asp129Glu) rs137852913
NM_139279.5(MCFD2):c.407T>C (p.Ile136Thr) rs137852914
NM_139279.5(MCFD2):c.416C>T (p.Ala139Val) rs80294301

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