ClinVar Miner

List of variants reported as benign for hypersensitivity reaction disease by Genome-Nilou Lab

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_000639.3(FASLG):c.452-28T>C rs2639653 0.99043
NM_006254.4(PRKCD):c.1857T>C (p.Pro619=) rs900495 0.94337
NM_006254.4(PRKCD):c.1782C>G (p.Thr594=) rs1075865 0.93819
NM_006254.4(PRKCD):c.1441C>T (p.Leu481=) rs2306574 0.75510
NM_006254.4(PRKCD):c.1743+29T>G rs7630600 0.74353
NM_000043.6(FAS):c.642T>C (p.Thr214=) rs2234978 0.72086
NM_006254.4(PRKCD):c.115+21C>G rs2306571 0.65337
NM_032977.4(CASP10):c.177A>G (p.Ser59=) rs3900115 0.49172
NM_032977.4(CASP10):c.1564T>A (p.Leu522Ile) rs13006529 0.42733
NM_006254.4(PRKCD):c.1119G>A (p.Glu373=) rs2230494 0.29106

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