ClinVar Miner

List of variants in gene FLCN reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP
NM_144997.7(FLCN):c.*178A>G rs145430714
NM_144997.7(FLCN):c.*442T>C rs7224213
NM_144997.7(FLCN):c.*526T>C rs574547835
NM_144997.7(FLCN):c.*528G>A rs184006653
NM_144997.7(FLCN):c.*634A>C rs199572622
NM_144997.7(FLCN):c.*911G>A rs571893996
NM_144997.7(FLCN):c.-141G>T rs541105214
NM_144997.7(FLCN):c.-176G>A rs117215381
NM_144997.7(FLCN):c.-29G>A rs151144873
NM_144997.7(FLCN):c.-431C>T rs138847774
NM_144997.7(FLCN):c.-45A>G rs571154058
NM_144997.7(FLCN):c.-480G>C rs564584154
NM_144997.7(FLCN):c.1062+8G>C rs1317761101
NM_144997.7(FLCN):c.1155G>A (p.Gln385=) rs141250189
NM_144997.7(FLCN):c.1269C>T (p.His423=) rs41464156
NM_144997.7(FLCN):c.1275G>A (p.Gln425=) rs1555607680
NM_144997.7(FLCN):c.1284C>G (p.Pro428=) rs942763423
NM_144997.7(FLCN):c.1300+14C>T rs200823760
NM_144997.7(FLCN):c.1300+8C>T rs936407961
NM_144997.7(FLCN):c.1332C>T (p.Ala444=) rs141283741
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr) rs41419545
NM_144997.7(FLCN):c.1359G>A (p.Gly453=) rs752677061
NM_144997.7(FLCN):c.1470G>A (p.Leu490=) rs1306737502
NM_144997.7(FLCN):c.1503C>T (p.Asp501=) rs1447641168
NM_144997.7(FLCN):c.1538+14T>G rs112111994
NM_144997.7(FLCN):c.225G>T (p.Gly75=) rs1555611381
NM_144997.7(FLCN):c.249+13G>C rs200103733
NM_144997.7(FLCN):c.276C>T (p.His92=) rs1555610970
NM_144997.7(FLCN):c.354C>T (p.Phe118=) rs1555610913
NM_144997.7(FLCN):c.456C>T (p.Phe152=) rs763630763
NM_144997.7(FLCN):c.591C>T (p.Ile197=) rs763617124
NM_144997.7(FLCN):c.597G>A (p.Glu199=) rs1555610215
NM_144997.7(FLCN):c.618+8C>G rs1555610185
NM_144997.7(FLCN):c.715C>T (p.Arg239Cys) rs78683075
NM_144997.7(FLCN):c.792G>T (p.Ala264=) rs140500421
NM_144997.7(FLCN):c.810C>A (p.Thr270=) rs372342796
NM_144997.7(FLCN):c.810C>G (p.Thr270=) rs372342796
NM_144997.7(FLCN):c.871+47G>A rs142934950
NM_144997.7(FLCN):c.872-11_872-10del rs1555608679
NM_144997.7(FLCN):c.882G>A (p.Glu294=) rs1555608661
NM_144997.7(FLCN):c.939G>A (p.Leu313=) rs558365108
NM_144997.7(FLCN):c.959G>A (p.Arg320Gln) rs143483053

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