ClinVar Miner

List of variants in gene MSX2 reported as likely benign for bone disorder

Included ClinVar conditions (1416):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_002449.5(MSX2):c.23A>G (p.Asn8Ser) rs367636705 0.00027
NM_002449.5(MSX2):c.379+7G>C rs569601106 0.00008
NM_002449.5(MSX2):c.380-11C>G rs376158014 0.00008
NM_002449.5(MSX2):c.*1206T>C rs77229212 0.00006
NM_002449.5(MSX2):c.286G>T (p.Val96Leu) rs769329948 0.00006
NM_002449.5(MSX2):c.*46G>T rs375964205 0.00005
NM_002449.5(MSX2):c.380-9G>C rs769673082 0.00004
NM_002449.5(MSX2):c.465C>T (p.Leu155=) rs1454617675 0.00004
NM_002449.5(MSX2):c.-42C>T rs758437365 0.00003
NM_002449.5(MSX2):c.255C>T (p.Gly85=) rs367614252 0.00003
NM_002449.5(MSX2):c.379+9G>A rs766596963 0.00003
NM_002449.5(MSX2):c.484C>T (p.Arg162Cys) rs555293970 0.00003
NM_002449.5(MSX2):c.591G>A (p.Ala197=) rs150352201 0.00003
NM_002449.5(MSX2):c.683C>T (p.Ser228Leu) rs373857075 0.00003
NM_002449.5(MSX2):c.749C>T (p.Pro250Leu) rs374244313 0.00003
NM_002449.5(MSX2):c.252C>T (p.His84=) rs531764887 0.00002
NM_002449.5(MSX2):c.803A>G (p.Ter268=) rs1436220047 0.00002
NM_002449.5(MSX2):c.174G>A (p.Pro58=) rs1234123597 0.00001
NM_002449.5(MSX2):c.213G>T (p.Ser71=) rs889301558 0.00001
NM_002449.5(MSX2):c.228G>A (p.Leu76=) rs999180495 0.00001
NM_002449.5(MSX2):c.315G>C (p.Lys105Asn) rs760574628 0.00001
NM_002449.5(MSX2):c.360C>T (p.Gly120=) rs778509123 0.00001
NM_002449.5(MSX2):c.39C>T (p.Pro13=) rs766427771 0.00001
NM_002449.5(MSX2):c.501C>T (p.Leu167=) rs752218690 0.00001
NM_002449.5(MSX2):c.750G>A (p.Pro250=) rs760404926 0.00001
NM_002449.5(MSX2):c.762C>G (p.Leu254=) rs560807345 0.00001
NM_002449.5(MSX2):c.771G>A (p.Thr257=) rs756385707 0.00001
NM_002449.5(MSX2):c.798G>C (p.Leu266=) rs2480603888 0.00001
NM_002449.5(MSX2):c.*1086dup rs145784193
NM_002449.5(MSX2):c.177C>T (p.Pro59=) rs2480592243
NM_002449.5(MSX2):c.22A>C (p.Asn8His) rs1760735062
NM_002449.5(MSX2):c.235C>T (p.Leu79=) rs1760746212
NM_002449.5(MSX2):c.282G>T (p.Pro94=)
NM_002449.5(MSX2):c.357C>G (p.Pro119=) rs756992471
NM_002449.5(MSX2):c.379+11G>A rs1373121328
NM_002449.5(MSX2):c.379+13C>T rs774294067
NM_002449.5(MSX2):c.379+8C>G rs1382294618
NM_002449.5(MSX2):c.380-14T>A
NM_002449.5(MSX2):c.380-16T>A rs1207193625
NM_002449.5(MSX2):c.380-17CT[3] rs1282197778
NM_002449.5(MSX2):c.380-18C>G rs200429446
NM_002449.5(MSX2):c.386_387inv (p.Met129Thr)
NM_002449.5(MSX2):c.441G>A (p.Thr147=)
NM_002449.5(MSX2):c.474G>A (p.Glu158=) rs2480603100
NM_002449.5(MSX2):c.501C>A (p.Leu167=)
NM_002449.5(MSX2):c.528C>T (p.Ser176=) rs2480603279
NM_002449.5(MSX2):c.597A>G (p.Arg199=) rs2480603382
NM_002449.5(MSX2):c.615G>A (p.Leu205=)

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