ClinVar Miner

List of variants reported as not provided for hypersensitivity reaction disease by GeneReviews

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_032977.4(CASP10):c.1228G>A (p.Val410Ile) rs13010627 0.04350
NM_032977.4(CASP10):c.1337A>G (p.Tyr446Cys) rs17860405 0.02926
NM_032977.4(CASP10):c.1216A>T (p.Ile406Leu) rs80358239 0.00307
NM_032977.4(CASP10):c.853C>T (p.Leu285Phe) rs17860403 0.00020
NM_000639.3(FASLG):c.466A>G (p.Arg156Gly) rs80358238 0.00010
NM_000639.3(FASLG):c.740C>A (p.Ala247Glu) rs80358237 0.00001
NM_000639.3(FASLG):c.829G>A (p.Gly277Ser) rs1413244355 0.00001
NM_000639.3(FASLG):c.203dup (p.Pro69fs) rs2101806549
NM_000639.3(FASLG):c.263del (p.Phe88fs) rs587776450
NM_000639.3(FASLG):c.473_556del (p.Met158_Glu185del) rs80358236
NM_000639.3(FASLG):c.605G>C (p.Cys202Ser) rs2101810634

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