List of variants reported as likely benign for hypersensitivity reaction disease by Illumina Laboratory Services, Illumina

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Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_001372051.1(CASP8):c.*71G>A	rs41309822	0.00687
NM_001141945.3(ACTA2):c.-24+357C>T	rs9658677	0.00433
NM_001372051.1(CASP8):c.*166G>C	rs35474602	0.00369
NM_001141945.3(ACTA2):c.-24+409G>A	rs56220100	0.00346
NM_001372051.1(CASP8):c.339C>T (p.Ser113=)	rs17860422	0.00309
NM_032977.4(CASP10):c.1216A>T (p.Ile406Leu)	rs80358239	0.00307
NM_001372051.1(CASP8):c.655T>A (p.Ser219Thr)	rs35976359	0.00241
NM_000043.6(FAS):c.580G>A (p.Glu194Lys)	rs56006128	0.00138
NM_000043.6(FAS):c.*436C>T	rs143388574	0.00132
NM_001372051.1(CASP8):c.*755G>A	rs145519245	0.00106
NM_032977.4(CASP10):c.1502C>T (p.Pro501Leu)	rs148939095	0.00091
NM_000639.3(FASLG):c.174G>A (p.Pro58=)	rs372411796	0.00034
NM_000043.6(FAS):c.*978C>T	rs181225729	0.00032
NM_032977.4(CASP10):c.913A>G (p.Lys305Glu)	rs149912574	0.00015
NM_000043.6(FAS):c.*70G>C	rs80330323	0.00012
NM_000639.3(FASLG):c.278C>T (p.Ala93Val)	rs758796005	0.00005
NM_000639.3(FASLG):c.*32T>C	rs775421228	0.00004
NM_000639.3(FASLG):c.-16T>C	rs781373207	0.00004
NM_000639.3(FASLG):c.176C>T (p.Pro59Leu)	rs375737004	0.00004
NM_032977.4(CASP10):c.1466G>A (p.Arg489Gln)	rs535121774	0.00004
NM_000043.6(FAS):c.867A>C (p.Glu289Asp)	rs377337130	0.00003
NM_032977.4(CASP10):c.1350G>T (p.Arg450=)	rs370670949	0.00003
NM_032977.4(CASP10):c.879C>A (p.Ser293Arg)	rs369897442	0.00003
NM_032977.4(CASP10):c.721G>A (p.Gly241Ser)	rs779013005	0.00001
NM_001141945.3(ACTA2):c.-24+414_-24+415del	rs553556054
NM_032977.3(CASP10):c.-285C>T	rs530526445
NM_032977.4(CASP10):c.*2177del	rs528903184
NM_032977.4(CASP10):c.*741del	rs41506545
NM_032977.4(CASP10):c.923-12del	rs367989998

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