ClinVar Miner

List of variants in gene TNFRSF11B reported as uncertain significance for bone remodeling disease

Included ClinVar conditions (104):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_002546.3(TNFRSF11B):c.-284C>T rs11575929 0.00457
NM_002546.4(TNFRSF11B):c.*67C>T rs11573944 0.00356
NM_002546.3(TNFRSF11B):c.-257G>T rs368831724 0.00255
NM_002546.4(TNFRSF11B):c.*682T>C rs189721016 0.00227
NM_002546.4(TNFRSF11B):c.234C>T (p.Asp78=) rs144654126 0.00081
NM_002546.4(TNFRSF11B):c.*609G>A rs529941362 0.00052
NM_002546.4(TNFRSF11B):c.700G>A (p.Ala234Thr) rs201393730 0.00047
NM_002546.4(TNFRSF11B):c.96C>T (p.Asp32=) rs4876870 0.00022
NM_002546.4(TNFRSF11B):c.840C>T (p.Ser280=) rs143414212 0.00021
NM_002546.4(TNFRSF11B):c.104C>A (p.Thr35Asn) rs150777320 0.00014
NM_002546.4(TNFRSF11B):c.332G>A (p.Arg111His) rs200629343 0.00009
NM_002546.4(TNFRSF11B):c.853A>G (p.Ile285Val) rs373848556 0.00009
NM_002546.3(TNFRSF11B):c.-311G>T rs779000439 0.00008
NM_002546.4(TNFRSF11B):c.621C>T (p.Phe207=) rs376708982 0.00008
NM_002546.4(TNFRSF11B):c.277G>A (p.Val93Ile) rs369646136 0.00007
NM_002546.4(TNFRSF11B):c.729A>T (p.Gln243His) rs374594601 0.00006
NM_002546.4(TNFRSF11B):c.*213C>T rs569762226 0.00004
NM_002546.4(TNFRSF11B):c.*349T>A rs888097904 0.00004
NM_002546.4(TNFRSF11B):c.-10G>A rs752426445 0.00004
NM_002546.4(TNFRSF11B):c.308G>A (p.Arg103His) rs375274060 0.00004
NM_002546.4(TNFRSF11B):c.400+5G>A rs372860364 0.00003
NM_002546.4(TNFRSF11B):c.400+15G>A rs757467378 0.00002
NM_002546.3(TNFRSF11B):c.-191C>G rs886062648 0.00001
NM_002546.3(TNFRSF11B):c.-99G>A rs886062647 0.00001
NM_002546.4(TNFRSF11B):c.*487T>C rs1421622252 0.00001
NM_002546.4(TNFRSF11B):c.*505A>G rs1812213517 0.00001
NM_002546.4(TNFRSF11B):c.*799G>A rs1397220907 0.00001
NM_002546.4(TNFRSF11B):c.720A>G (p.Ile240Met) rs767927201 0.00001
NM_002546.3(TNFRSF11B):c.-204C>T rs570347828
NM_002546.3(TNFRSF11B):c.-215C>T rs886062649
NM_002546.4(TNFRSF11B):c.*166C>G rs1812218708
NM_002546.4(TNFRSF11B):c.*207C>G rs886062646
NM_002546.4(TNFRSF11B):c.*412A>G rs1379870216
NM_002546.4(TNFRSF11B):c.*463T>A rs574050965
NM_002546.4(TNFRSF11B):c.139G>A (p.Gly47Ser) rs1812353362
NM_002546.4(TNFRSF11B):c.699C>A (p.Asn233Lys) rs150457771
NM_002546.4(TNFRSF11B):c.841G>T (p.Val281Leu) rs140782326
NM_002546.4(TNFRSF11B):c.884T>C (p.Leu295Pro) rs1586952570
NM_002546.4(TNFRSF11B):c.97G>A (p.Glu33Lys) rs202090603

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