ClinVar Miner

List of variants in gene FECH reported as likely benign for digestive system disorder

Included ClinVar conditions (605):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_000140.5(FECH):c.*571G>A rs114617188 0.01460
NM_000140.5(FECH):c.*892T>C rs13271 0.01039
NM_000140.5(FECH):c.*5801T>G rs139119026 0.00849
NM_000140.5(FECH):c.*5394G>T rs145935279 0.00711
NM_000140.5(FECH):c.*4458C>T rs113000324 0.00623
NM_000140.5(FECH):c.*3841C>T rs143797631 0.00586
NM_000140.5(FECH):c.*4883_*4884insC rs201434287 0.00582
NM_000140.5(FECH):c.*1479T>C rs112062178 0.00287
NM_000140.5(FECH):c.*3567G>A rs556538397 0.00273
NM_000140.5(FECH):c.*4597T>C rs147684323 0.00237
NM_000140.5(FECH):c.*2788G>A rs145954113 0.00234
NM_000140.5(FECH):c.*936C>T rs144709743 0.00200
NM_000140.5(FECH):c.*347G>A rs113392534 0.00192
NM_000140.5(FECH):c.*4056C>T rs181920623 0.00166
NM_000140.5(FECH):c.*3339G>A rs113928110 0.00159
NM_000140.5(FECH):c.*4367C>T rs146417207 0.00112
NM_000140.5(FECH):c.801G>A (p.Met267Ile) rs118204037 0.00108
NM_000140.5(FECH):c.*3804G>A rs190604320 0.00107
NM_000140.5(FECH):c.*4829C>T rs565989254 0.00093
NM_000140.5(FECH):c.*1915G>T rs148459563 0.00067
NM_000140.5(FECH):c.*4445G>A rs578202706 0.00053
NM_000140.5(FECH):c.*1508G>A rs540286571 0.00048
NM_000140.5(FECH):c.*1567A>G rs574153215 0.00044
NM_000140.5(FECH):c.362A>G (p.Glu121Gly) rs141813907 0.00043
NM_000140.5(FECH):c.*1032G>A rs140863287 0.00034
NM_000140.5(FECH):c.*2443T>G rs201834035 0.00034
NM_000140.5(FECH):c.913-13A>G rs200538834 0.00022
NM_000140.5(FECH):c.*1054T>C rs192343321 0.00020
NM_000140.5(FECH):c.*2644A>G rs558443758 0.00016
NM_000140.5(FECH):c.132C>T (p.Ala44=) rs147500247 0.00015
NM_000140.5(FECH):c.385G>A (p.Gly129Arg) rs138714094 0.00010
NM_000140.5(FECH):c.*3691C>T rs148141502 0.00008
NM_000140.5(FECH):c.*3716C>T rs567960865 0.00005
NM_000140.5(FECH):c.514G>A (p.Glu172Lys) rs200650502 0.00001
NM_000140.5(FECH):c.*1039G>A rs185134664
NM_000140.5(FECH):c.*2840C>T rs568628377
NM_000140.5(FECH):c.*4368G>A rs543603003
NM_000140.5(FECH):c.*4793TTA[1] rs137860528
NM_000140.5(FECH):c.*592C>T rs577112809
NM_000140.5(FECH):c.163G>T (p.Gly55Cys) rs3848519

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