ClinVar Miner

List of variants in gene combination ACER2, ADAMTSL1, BNC2, CCDC171, CDKN2A, CDKN2B, CER1, CNTLN, DENND4C, DMRTA1, ELAVL2, FOCAD, FREM1, HACD4, HAUS6, IFNA1, IFNA10, IFNA13, IFNA14, IFNA16, IFNA17, IFNA2, IFNA21, IFNA4, IFNA5, IFNA6, IFNA7, IFNA8, IFNB1, IFNE, IFNW1, IZUMO3, KLHL9, LURAP1L, MIR31, MLLT3, MPDZ, MTAP, NFIB, PLIN2, PSIP1, PTPRD, RPS6, RRAGA, SAXO1, SH3GL2, SLC24A2, SNAPC3, TTC39B, TUSC1, TYRP1, ZDHHC21 reported as drug response by Oxford Haemato-Oncology Service, Oxford University Hospitals NHS Foundation Trust

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 9p23-21.2(chr9:10320113-26205565)x1

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