ClinVar Miner

List of variants in gene SNAP29 reported as benign for autosomal ichthyosis syndrome

Included ClinVar conditions (42):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP
NM_004782.4(SNAP29):c.*1129T>C rs165801
NM_004782.4(SNAP29):c.*123G>C rs3171741
NM_004782.4(SNAP29):c.*138C>T rs375995790
NM_004782.4(SNAP29):c.*1490T>C rs12168260
NM_004782.4(SNAP29):c.*1519T>C rs165861
NM_004782.4(SNAP29):c.*1563T>G rs11577
NM_004782.4(SNAP29):c.*2105T>G rs5752201
NM_004782.4(SNAP29):c.*2261G>T rs165744
NM_004782.4(SNAP29):c.*2551G>A rs73162856
NM_004782.4(SNAP29):c.*2692C>T rs148419415
NM_004782.4(SNAP29):c.*2783C>T rs142566638
NM_004782.4(SNAP29):c.*2791T>C rs187911143
NM_004782.4(SNAP29):c.*2795C>T rs9625042
NM_004782.4(SNAP29):c.*2796G>A
NM_004782.4(SNAP29):c.*2816A>G rs165739
NM_004782.4(SNAP29):c.*2856G>A rs9625044
NM_004782.4(SNAP29):c.*2872G>A rs111581119
NM_004782.4(SNAP29):c.*2879C>T rs140626919
NM_004782.4(SNAP29):c.*2892C>T
NM_004782.4(SNAP29):c.*2961T>C rs165715
NM_004782.4(SNAP29):c.*3015G>A rs145199625
NM_004782.4(SNAP29):c.*420A>G rs178077
NM_004782.4(SNAP29):c.*521T>A rs361998
NM_004782.4(SNAP29):c.*740C>T rs79383799
NM_004782.4(SNAP29):c.*755A>G
NM_004782.4(SNAP29):c.-19C>T rs1061063
NM_004782.4(SNAP29):c.-32C>G rs202138036
NM_004782.4(SNAP29):c.-5G>A rs139884576
NM_004782.4(SNAP29):c.-68A>T rs117593372
NM_004782.4(SNAP29):c.-8C>G rs186825747
NM_004782.4(SNAP29):c.130T>C (p.Tyr44His) rs116644127
NM_004782.4(SNAP29):c.18A>G (p.Lys6=) rs1061064
NM_004782.4(SNAP29):c.265G>A (p.Glu89Lys) rs151146863
NM_004782.4(SNAP29):c.487A>G (p.Ser163Gly) rs116892729
NM_004782.4(SNAP29):c.72T>A (p.Pro24=) rs149837436

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