ClinVar Miner

List of variants in gene TNFSF11 studied for autosomal recessive disease

Included ClinVar conditions (1198):
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Gene type:
ClinVar version:
Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_003701.4(TNFSF11):c.*264G>T rs346575 0.99437
NM_003701.4(TNFSF11):c.*948G>T rs1054016 0.36610
NM_003701.4(TNFSF11):c.924T>C (p.Phe308=) rs9562415 0.03075
NM_003701.4(TNFSF11):c.*48T>C rs7994018 0.02917
NM_003701.4(TNFSF11):c.*383C>T rs9567000 0.02228
NM_003701.4(TNFSF11):c.*704G>A rs34886516 0.00933
NM_003701.4(TNFSF11):c.*742G>A rs139327529 0.00897
NM_003701.4(TNFSF11):c.*745T>C rs12721444 0.00615
NM_003701.4(TNFSF11):c.214G>A (p.Ala72Thr) rs142756983 0.00164
NM_003701.4(TNFSF11):c.*788T>C rs200189539 0.00135
NM_003701.4(TNFSF11):c.534T>C (p.Gly178=) rs146484645 0.00024
NM_003701.4(TNFSF11):c.*159G>A rs186999111 0.00013
NM_003701.4(TNFSF11):c.*357C>T rs192340175 0.00011
NM_003701.4(TNFSF11):c.*158C>T rs200754328 0.00008
NM_003701.4(TNFSF11):c.*754A>C rs924942406 0.00006
NM_003701.4(TNFSF11):c.*667A>G rs12584726 0.00005
NM_003701.4(TNFSF11):c.845A>C (p.Lys282Thr) rs201151635 0.00005
NM_003701.4(TNFSF11):c.*554A>G rs200749870 0.00003
NM_003701.4(TNFSF11):c.849A>G (p.Leu283=) rs199769531 0.00002
NM_003701.4(TNFSF11):c.*113G>A rs886050253 0.00001
NM_003701.4(TNFSF11):c.*152A>G rs886050254 0.00001
NM_003701.4(TNFSF11):c.533-8C>T rs1869458758 0.00001
NM_003701.4(TNFSF11):c.851G>A (p.Arg284Gln) rs61761332 0.00001
NM_003701.4(TNFSF11):c.*119C>T rs200387399
NM_003701.4(TNFSF11):c.*221G>C rs1315042884
NM_003701.4(TNFSF11):c.*242A>G rs1594485076
NM_003701.4(TNFSF11):c.*261G>A rs995293287
NM_003701.4(TNFSF11):c.*94T>G rs886050252
NM_003701.4(TNFSF11):c.596T>A (p.Met199Lys) rs121909072
NM_003701.4(TNFSF11):c.618A>G (p.Leu206=) rs770524066
NM_003701.4(TNFSF11):c.667C>T (p.Arg223Ter) rs267603829
NM_003701.4(TNFSF11):c.828_829del (p.Val277fs) rs863223288
NM_003701.4(TNFSF11):c.911A>G (p.Asp304Gly) rs760748407
NM_003701.4(TNFSF11):c.929del (p.Ala310fs) rs2137916719

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