ClinVar Miner

List of variants in gene TINF2 reported as likely benign for anemia (disease)

Included ClinVar conditions (262):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP
NM_001099274.3(TINF2):c.-161G>A rs577503785
NM_001099274.3(TINF2):c.-172A>C rs11557911
NM_001099274.3(TINF2):c.-225G>A rs35781178
NM_001099274.3(TINF2):c.-266G>A rs35886534
NM_001099274.3(TINF2):c.-91C>T rs36124829
NM_001099274.3(TINF2):c.1092G>A (p.Leu364=) rs184422577
NM_001099274.3(TINF2):c.1166T>C (p.Ile389Thr) rs192423622
NM_001099274.3(TINF2):c.1236C>T (p.Asn412=) rs117234138
NM_001099274.3(TINF2):c.1290C>G (p.Pro430=) rs201083863
NM_001099274.3(TINF2):c.159C>T (p.His53=) rs370875792
NM_001099274.3(TINF2):c.359A>G (p.Gln120Arg) rs189265179
NM_001099274.3(TINF2):c.45C>T (p.Ala15=) rs750285418
NM_001099274.3(TINF2):c.520C>T (p.Leu174=) rs374116388
NM_001099274.3(TINF2):c.706C>T (p.Pro236Ser) rs199422321
NM_001099274.3(TINF2):c.734C>A (p.Ser245Tyr) rs142777869
NM_001099274.3(TINF2):c.74G>C (p.Gly25Ala) rs202093758
NM_001099274.3(TINF2):c.771C>T (p.His257=) rs75124018
NM_001099274.3(TINF2):c.841G>A (p.Glu281Lys) rs199422322
NM_012461.3(TINF2):c.*709T>C rs183352266

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