ClinVar Miner

List of variants in gene SOST studied for bone disorder

Included ClinVar conditions (1346):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_025237.3(SOST):c.*1004G>A rs17886183 0.10131
NM_025237.3(SOST):c.*1394C>G rs75335214 0.09237
NM_025237.3(SOST):c.*866C>T rs75901553 0.04189
NM_025237.3(SOST):c.*320C>T rs17883310 0.01264
NM_025237.3(SOST):c.28G>A (p.Val10Ile) rs17882143 0.01107
NM_025237.3(SOST):c.*562G>A rs17881518 0.00905
NM_025237.3(SOST):c.*178C>T rs116799821 0.00690
NM_025237.3(SOST):c.*222A>G rs544576964 0.00346
NM_025237.3(SOST):c.-21T>G rs202008449 0.00319
NM_025237.3(SOST):c.-10G>A rs190743758 0.00262
NM_025237.3(SOST):c.*1391G>C rs144304911 0.00249
NM_025237.3(SOST):c.*902T>C rs531006039 0.00096
NM_025237.3(SOST):c.153G>A (p.Glu51=) rs150640883 0.00039
NM_025237.3(SOST):c.*203G>A rs753407763 0.00018
NM_025237.3(SOST):c.*314C>G rs765892196 0.00013
NM_025237.3(SOST):c.56G>A (p.Arg19His) rs199514554 0.00011
NM_025237.3(SOST):c.*1529T>C rs182899606 0.00006
NM_025237.3(SOST):c.114C>T (p.Pro38=) rs750870565 0.00004
NM_025237.3(SOST):c.*219T>C rs1017350702 0.00003
NM_025237.3(SOST):c.*1267C>G rs76802447 0.00002
NM_025237.3(SOST):c.143C>T (p.Pro48Leu) rs779039644 0.00002
NM_025237.3(SOST):c.177G>A (p.Ala59=) rs201706408 0.00002
NM_025237.3(SOST):c.*1176A>G rs886052978 0.00001
NM_025237.3(SOST):c.*1498G>A rs866808140 0.00001
NM_025237.3(SOST):c.*666T>C rs538476059 0.00001
NM_025237.3(SOST):c.303C>T (p.Thr101=) rs758794256 0.00001
NM_025237.3(SOST):c.328G>A (p.Gly110Ser) rs886052981 0.00001
NM_025237.3(SOST):c.461C>T (p.Pro154Leu) rs760883576 0.00001
NM_025237.3(SOST):c.70C>T (p.Gln24Ter) rs387906320 0.00001
NM_025237.3(SOST):c.*1063C>T rs1352568425
NM_025237.3(SOST):c.*1363C>T rs918885949
NM_025237.3(SOST):c.*1402T>G rs1974097858
NM_025237.3(SOST):c.*140A>G rs886052979
NM_025237.3(SOST):c.*569G>T rs1974108139
NM_025237.3(SOST):c.*689T>C rs1470510281
NM_025237.3(SOST):c.*883A>T rs1974104389
NM_025237.3(SOST):c.220+1G>C rs952785856
NM_025237.3(SOST):c.220+3A>T rs2154590472
NM_025237.3(SOST):c.296dup (p.Val100fs) rs1974122996
NM_025237.3(SOST):c.327C>A (p.Cys109Ter)
NM_025237.3(SOST):c.371G>A (p.Trp124Ter) rs2154590429
NM_025237.3(SOST):c.372G>A (p.Trp124Ter) rs104894644
NM_025237.3(SOST):c.376C>T (p.Arg126Ter) rs104894645
NM_025237.3(SOST):c.444_445delinsAA (p.Cys148_Pro149delinsTer) rs2154590427
NM_025237.3(SOST):c.448G>A (p.Gly150Ser) rs548849329
NM_025237.3(SOST):c.499T>C (p.Cys167Arg) rs2154590425
NM_025237.3(SOST):c.533A>G (p.Glu178Gly) rs886052980
NM_025237.3(SOST):c.61G>A (p.Val21Met) rs387907169
NM_025237.3(SOST):c.61G>T (p.Val21Leu) rs387907169
NM_025237.3(SOST):c.69C>T (p.Gly23=) rs1461545319
NM_025237.3(SOST):c.79C>T (p.Gln27Ter) rs2154590473
NM_025237.3(SOST):c.87dup (p.Lys30fs) rs377648601
NM_025237.3(SOST):c.[220+3A>T;221-67A>C]

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