ClinVar Miner

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

Included ClinVar conditions (69):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_139279.6(MCFD2):c.*1995G>A rs183896754 0.00603
NM_139279.6(MCFD2):c.*1111G>C rs181922575 0.00461
NM_139279.6(MCFD2):c.*2056T>G rs145495352 0.00421
NM_139279.6(MCFD2):c.*1415C>T rs147096932 0.00317
NM_139279.6(MCFD2):c.*2848C>T rs142254354 0.00248
NM_139279.6(MCFD2):c.*517C>G rs761766519 0.00228
NM_139279.6(MCFD2):c.*84T>C rs182576601 0.00207
NM_139279.6(MCFD2):c.*2423A>G rs139408737 0.00120
NM_001171506.2(MCFD2):c.*3591C>G rs78040887 0.00115
NM_139279.6(MCFD2):c.*3272A>G rs148722702 0.00110
NM_139279.6(MCFD2):c.*64T>C rs754447509 0.00102
NM_139279.6(MCFD2):c.*1314C>T rs150644996 0.00093
NM_139279.6(MCFD2):c.-7+11T>A rs201752014 0.00070
NM_139279.6(MCFD2):c.*912C>T rs189018618 0.00040
NM_139279.6(MCFD2):c.*62T>G rs886056117 0.00031
NM_139279.6(MCFD2):c.*1875T>C rs552695942 0.00021
NM_139279.6(MCFD2):c.*1187C>T rs550737178 0.00016
NM_139279.6(MCFD2):c.*2017C>T rs886056111 0.00016
NM_139279.6(MCFD2):c.*2843T>A rs559142075 0.00016
NM_139279.6(MCFD2):c.*3014G>A rs886056107 0.00016
NM_139279.6(MCFD2):c.*418C>G rs1043866618 0.00011
NM_139279.6(MCFD2):c.*3293A>C rs763634945 0.00010
NM_139279.6(MCFD2):c.*2121G>A rs187335799 0.00006
NM_139279.6(MCFD2):c.*2983T>C rs1316076292 0.00006
NM_139279.6(MCFD2):c.*1158C>A rs886056113 0.00005
NM_139279.6(MCFD2):c.*2128C>T rs1030805726 0.00005
NM_139279.6(MCFD2):c.*2556C>T rs1009835953 0.00005
NM_139279.6(MCFD2):c.*445A>G rs1160902939 0.00005
NM_139279.6(MCFD2):c.*1151G>C rs761404637 0.00004
NM_139279.6(MCFD2):c.*311G>A rs886056115 0.00003
NM_139279.6(MCFD2):c.*375T>C rs957621417 0.00003
NM_139279.6(MCFD2):c.106C>G (p.Pro36Ala) rs756021929 0.00003
NM_139279.6(MCFD2):c.416C>T (p.Ala139Val) rs80294301 0.00003
NM_139279.6(MCFD2):c.*1289T>C rs527427772 0.00002
NM_139279.6(MCFD2):c.*1354G>T rs886056112 0.00002
NM_139279.6(MCFD2):c.*2169G>A rs79487300 0.00002
NM_139279.6(MCFD2):c.*428G>A rs781195000 0.00002
NM_139279.6(MCFD2):c.*640C>T rs534106665 0.00002
NM_139279.6(MCFD2):c.*991G>A rs1259504368 0.00002
NM_139279.6(MCFD2):c.*1024C>T rs1668136066 0.00001
NM_139279.6(MCFD2):c.*1079C>T rs980914930 0.00001
NM_139279.6(MCFD2):c.*1316G>T rs1301628664 0.00001
NM_139279.6(MCFD2):c.*1448G>A rs1041505834 0.00001
NM_139279.6(MCFD2):c.*1537G>C rs1280227531 0.00001
NM_139279.6(MCFD2):c.*1610A>T rs1668107899 0.00001
NM_139279.6(MCFD2):c.*173G>T rs886056116 0.00001
NM_139279.6(MCFD2):c.*2647A>C rs374313566 0.00001
NM_139279.6(MCFD2):c.*2760G>T rs1403622431 0.00001
NM_139279.6(MCFD2):c.*2789G>C rs886056108 0.00001
NM_139279.6(MCFD2):c.*648C>T rs1468272258 0.00001
NM_139279.6(MCFD2):c.138G>A (p.Val46=) rs766859640 0.00001
NM_139279.6(MCFD2):c.236T>C (p.Met79Thr) rs886056118 0.00001
NM_139279.6(MCFD2):c.321A>G (p.Glu107=) rs1322883135 0.00001
NM_139279.6(MCFD2):c.363A>G (p.Ile121Met) rs768388209 0.00001
NM_139279.6(MCFD2):c.*1059C>G rs1420248449
NM_139279.6(MCFD2):c.*1464A>G rs1207325090
NM_139279.6(MCFD2):c.*1867C>A rs1558458280
NM_139279.6(MCFD2):c.*2106T>G rs1668088874
NM_139279.6(MCFD2):c.*2141G>C rs546151221
NM_139279.6(MCFD2):c.*217T>G rs746370141
NM_139279.6(MCFD2):c.*2436G>T rs535350829
NM_139279.6(MCFD2):c.*2565A>G rs886056110
NM_139279.6(MCFD2):c.*2780_*2781del rs886056109
NM_139279.6(MCFD2):c.*3072_*3073insGG rs559484016
NM_139279.6(MCFD2):c.*3099G>A rs886056106
NM_139279.6(MCFD2):c.*3354A>G rs886056105
NM_139279.6(MCFD2):c.*422T>C rs1668160546
NM_139279.6(MCFD2):c.*529G>A rs542831100
NM_139279.6(MCFD2):c.*632T>C rs1668150921
NM_139279.6(MCFD2):c.*751G>A rs544942135
NM_139279.6(MCFD2):c.*79A>G rs1572605422
NM_139279.6(MCFD2):c.*892G>A rs886056114
NM_139279.6(MCFD2):c.-34C>A rs886056119
NM_139279.6(MCFD2):c.108C>A (p.Pro36=) rs767456045
NM_139279.6(MCFD2):c.47T>C (p.Leu16Pro) rs1572611822

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