ClinVar Miner

List of variants in gene LOC130009662, TNFSF11 studied for bone disorder

Included ClinVar conditions (1436):
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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_003701.4(TNFSF11):c.-127C>G rs9533157 0.99807
NM_003701.4(TNFSF11):c.126T>C (p.Pro42=) rs2296533 0.46914
NM_003701.4(TNFSF11):c.107C>G (p.Pro36Arg) rs138818878 0.02149
NM_003701.4(TNFSF11):c.147C>T (p.Phe49=) rs61735535 0.00938
NM_003701.4(TNFSF11):c.45G>A (p.Ser15=) rs200121871 0.00316
NM_003701.4(TNFSF11):c.-94C>T rs199818393 0.00272
NM_003701.4(TNFSF11):c.80A>G (p.Glu27Gly) rs200788562 0.00262
NM_003701.4(TNFSF11):c.-144G>C rs201859220 0.00188
NM_003701.4(TNFSF11):c.98C>A (p.Pro33Gln) rs200250962 0.00143
NM_003701.4(TNFSF11):c.-81C>A rs200647526 0.00120
NM_003701.4(TNFSF11):c.-141C>T rs45468495 0.00067
NM_003701.4(TNFSF11):c.83G>A (p.Gly28Asp) rs201652399 0.00056
NM_003701.4(TNFSF11):c.-64C>G rs886050251 0.00003
NM_003701.4(TNFSF11):c.148G>A (p.Val50Met) rs779371056 0.00002
NM_003701.4(TNFSF11):c.-104C>T rs1873181204 0.00001
NM_003701.4(TNFSF11):c.-4C>T rs781185506 0.00001
NM_003701.4(TNFSF11):c.92A>T (p.His31Leu) rs1471498841 0.00001
NM_003701.4(TNFSF11):c.-147C>T rs1873177411
NM_003701.4(TNFSF11):c.-74C>T rs569615616
NM_003701.4(TNFSF11):c.-7G>C rs998463381
NM_003701.4(TNFSF11):c.2T>C (p.Met1Thr) rs201199211
NM_003701.4(TNFSF11):c.2T>G (p.Met1Arg) rs201199211

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