ClinVar Miner

List of variants reported as benign for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 50
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HGVS dbSNP
NM_000128.3(F11):c.*296G>C rs4253430
NM_000128.3(F11):c.*479A>T rs1062547
NM_000128.3(F11):c.*852G>A rs4253431
NM_000128.3(F11):c.-316C>G rs3733403
NM_000128.3(F11):c.1191T>C (p.Gly397=) rs5970
NM_000128.3(F11):c.801A>G (p.Thr267=) rs5974
NM_000129.3(F13A1):c.-19+12A>C rs2815822
NM_000131.4(F7):c.*770G>A rs3093253
NM_000131.4(F7):c.1238G>A (p.Arg413Gln) rs6046
NM_000131.4(F7):c.525C>T (p.His175=) rs6042
NM_000131.4(F7):c.64+9G>A rs6039
NM_000132.2:c.*8899A>G
NM_000132.3(F8):c.3780C>G (p.Asp1260Glu) rs1800291
NM_000132.3(F8):c.3864A>C (p.Ser1288=) rs1800292
NM_000132.3(F8):c.6769A>G (p.Met2257Val) rs1800297
NM_000133.3(F9):c.1095A>G (p.Ser365=) rs112057482
NM_000133.3(F9):c.1381A>C (p.Thr461Pro) rs4149751
NM_000133.3(F9):c.19A>T (p.Ile7Phe) rs150190385
NM_000133.3(F9):c.391+10T>G rs375734226
NM_000133.3(F9):c.391+7A>G rs6049
NM_000133.3(F9):c.819T>C (p.Val273=) rs1800455
NM_000504.4(F10):c.792C>T (p.Thr264=) rs5960
NM_000505.3(F12):c.-4T>C rs1801020
NM_000505.3(F12):c.1251-9C>T rs17876032
NM_000505.3(F12):c.619G>C (p.Ala207Pro) rs17876030
NM_000505.3(F12):c.711C>T (p.Pro237=) rs17876047
NM_000505.3(F12):c.756C>T (p.Ala252=) rs41309752
NM_000509.5(FGG):c.*216C>T rs2066865
NM_000602.4(SERPINE1):c.*1737G>A rs1050955
NM_000602.4(SERPINE1):c.*361T>C rs11178
NM_000602.4(SERPINE1):c.*722T>G rs7242
NM_000602.4(SERPINE1):c.*997_*1005dup rs41423845
NM_001171506.2(MCFD2):c.-198_-190del rs372282781
NM_001994.2(F13B):c.1806T>C (p.Asn602=) rs5998
NM_001994.2(F13B):c.344G>A (p.Arg115His) rs6003
NM_001994.2(F13B):c.456A>G (p.Thr152=) rs5997
NM_003052.5(SLC34A1):c.*202A>C rs6556319
NM_003052.5(SLC34A1):c.1635C>T (p.Gly545=) rs7379524
NM_005141.4(FGB):c.*1550C>T rs1044291
NM_005141.4(FGB):c.*422A>C rs2227421
NM_005141.4(FGB):c.*619T>C rs2227439
NM_005141.4(FGB):c.*834del rs57313183
NM_005141.4(FGB):c.567C>T (p.Ser189=) rs6056
NM_005141.4(FGB):c.959-13_959-10del rs140114081
NM_005570.4(LMAN1):c.*2929T>C rs4806
NM_021871.3(FGA):c.-58A>G rs2070011
NM_021871.4(FGA):c.16A>G (p.Ile6Val) rs2070025
NM_021871.4(FGA):c.991A>G (p.Thr331Ala) rs6050
NM_139279.5(MCFD2):c.*1267G>T rs7596245
NM_139279.5(MCFD2):c.*1752T>C rs6544935

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