ClinVar Miner

List of variants in gene TNNT2 reported as benign for cardiovascular disorder

Included ClinVar conditions (1426):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_001276345.2(TNNT2):c.163+120T>C rs3729842 0.84150
NM_001276345.2(TNNT2):c.601-32A>C rs1104859 0.73965
NM_001276345.2(TNNT2):c.348C>T (p.Ile116=) rs3729547 0.69444
NM_001276345.2(TNNT2):c.811-122C>G rs45509695 0.22049
NM_001276345.2(TNNT2):c.811-33C>T rs2275863 0.22049
NM_001276345.2(TNNT2):c.237G>A (p.Ser79=) rs3729845 0.08311
NM_001276345.2(TNNT2):c.788A>G (p.Lys263Arg) rs3730238 0.05965
NM_001276345.2(TNNT2):c.610-90G>A rs11810834 0.03251
NM_001276345.2(TNNT2):c.*66G>A rs3729998 0.01883
NM_001276345.2(TNNT2):c.163+12G>A rs45580032 0.01441
NM_001276345.2(TNNT2):c.42-20G>A rs45561443 0.01192
NM_001276345.2(TNNT2):c.294+7G>A rs45490292 0.01066
NM_001276345.2(TNNT2):c.68-8A>G rs115805892 0.00864
NM_001276345.2(TNNT2):c.610-81C>T rs28730745 0.00831
NM_001276345.2(TNNT2):c.474G>C (p.Arg158=) rs35914325 0.00788
NM_001276345.2(TNNT2):c.200-29C>G rs45449197 0.00690
NM_001276345.2(TNNT2):c.53-47C>G rs45553832 0.00345
NM_001276345.2(TNNT2):c.68-5C>T rs540630390 0.00133
NM_001276345.2(TNNT2):c.610-106C>T rs373805222 0.00113
NM_001276345.2(TNNT2):c.98-81G>A rs45576939 0.00067
NM_001276345.2(TNNT2):c.720-13_720-11del rs397516480 0.00031
NM_001276345.2(TNNT2):c.41+16A>G rs370729174 0.00029
NM_001276345.2(TNNT2):c.200-11A>G rs368658464 0.00021
NM_001276345.2(TNNT2):c.692T>C (p.Ile231Thr) rs45520032 0.00015
NM_001276345.2(TNNT2):c.295-19C>T rs587780969 0.00009
NM_001276345.2(TNNT2):c.720-4G>T rs201753429 0.00009
NM_001276345.2(TNNT2):c.52+7G>A rs374443596 0.00007
NM_001276345.2(TNNT2):c.114G>A (p.Ala38=) rs200283086 0.00006
NM_001276345.2(TNNT2):c.295-14C>T rs747477576 0.00006
NM_001276345.2(TNNT2):c.601-8C>T rs397516475 0.00006
NM_001276345.2(TNNT2):c.52+13G>A rs376820377 0.00004
NM_001276345.2(TNNT2):c.63T>G (p.Val21=) rs397516477 0.00002
NM_001276345.2(TNNT2):c.522C>T (p.Asn174=) rs483352833 0.00001
NM_001276345.2(TNNT2):c.163+12G>T rs45580032
NM_001276345.2(TNNT2):c.164-50G>A rs3729843
NM_001276345.2(TNNT2):c.237G>T (p.Ser79=) rs3729845
NM_001276345.2(TNNT2):c.270C>T (p.Pro90=) rs140245123
NM_001276345.2(TNNT2):c.351G>A (p.Glu117=) rs1659436211
NM_001276345.2(TNNT2):c.412-6_412-4del rs397516462
NM_001276345.2(TNNT2):c.412-94del rs35559054
NM_001276345.2(TNNT2):c.451C>A (p.Arg151=) rs74315379
NM_001276345.2(TNNT2):c.53-11_53-7del rs45533739
NM_001276345.2(TNNT2):c.53-12del rs730881094
NM_001276345.2(TNNT2):c.811-8del

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