ClinVar Miner

List of variants in gene combination STX16, STX16-NPEPL1 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (916):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP
NM_001001433.3(STX16):c.*1581G>C rs73302110
NM_001001433.3(STX16):c.*1785A>G rs6128397
NM_001001433.3(STX16):c.*183G>T rs1052642
NM_001001433.3(STX16):c.*1928C>T rs11578
NM_001001433.3(STX16):c.*2057G>A rs7683
NM_001001433.3(STX16):c.*2060T>C rs115404291
NM_001001433.3(STX16):c.*2365A>T rs189786439
NM_001001433.3(STX16):c.*3175_*3176del rs35295928
NM_001001433.3(STX16):c.*70G>A rs114597931
NM_001001433.3(STX16):c.-350C>A rs41296205
NM_001001433.3(STX16):c.141C>T (p.Asp47=) rs73598392
NM_001001433.3(STX16):c.443G>A (p.Arg148Gln) rs41276950
NM_001001433.3(STX16):c.540G>A (p.Gln180=) rs2296524
NR_037941.1(STX16):n.11T>C rs6026428

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