ClinVar Miner

List of variants in gene TTC37 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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NM_014639.3(TTC37):c.1783C>G (p.Pro595Ala) rs751343448
NM_014639.3(TTC37):c.2494G>T (p.Gly832Cys)
NM_014639.3(TTC37):c.3124G>C (p.Ala1042Pro) rs146638227
NM_014639.3(TTC37):c.3808C>G (p.Pro1270Ala) rs146627706
NM_014639.3(TTC37):c.3885G>T (p.Lys1295Asn) rs892221746
NM_014639.3(TTC37):c.4187A>G (p.Asn1396Ser) rs116690692
NM_014639.3(TTC37):c.4310G>T (p.Ser1437Ile) rs755895621
NM_014639.4(TTC37):c.2275C>T (p.Leu759Phe)

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