ClinVar Miner

List of variants in gene ACSF3, ADAD2, ADAMTS18, ADAT1, ANKRD11, APRT, ATMIN, ATP2C2, BANP, BCAR1, BCO1, C16orf46, C16orf47, C16orf74, C16orf95, CA5A, CBFA2T3, CDH13, CDH15, CDK10, CDT1, CDYL2, CENPBD1, CENPN, CFDP1, CHMP1A, CHST5, CHST6, CIBAR2, CLEC18B, CLEC3A, CMC2, CMIP, CNTNAP4, COTL1, COX4I1, CPNE7, CRISPLD2, CTRB1, CTRB2, CTU2, CYBA, DBNDD1, DEF8, DHX38, DNAAF1, DPEP1, DYNLRB2, EMC8, FA2H, FANCA, FBXO31, FENDRR, FOXC2, FOXF1, FOXL1, GABARAPL2, GALNS, GAN, GAS8, GCSH, GINS2, GLG1, GSE1, HPR, HSBP1, HSD17B2, HSDL1, IL17C, IRF8, JPH3, KARS1, KCNG4, KIAA0513, KLHDC4, KLHL36, LDHD, LINC01082, LOC101927817, LOC101928417, LOC654780, MAF, MAP1LC3B, MBTPS1, MC1R, MEAK7, MLKL, MLYCD, MON1B, MPHOSPH6, MTHFSD, MVD, NECAB2, NPIPB15, NUDT7, OSGIN1, PABPN1L, PIEZO1, PKD1L2, PLCG2, PMFBP1, PRDM7, PSMD7, RFWD3, RNF166, RPL13, SDR42E1, SLC22A31, SLC38A8, SLC7A5, SNAI3, SPATA2L, SPATA33, SPG7, SPIRE2, SYCE1L, TAF1C, TCF25, TERF2IP, TMEM170A, TMEM231, TRAPPC2L, TUBB3, TXNL4B, USP10, VAT1L, VPS9D1, WDR59, WFDC1, WWOX, ZC3H18, ZCCHC14, ZCCHC14-DT, ZDHHC7, ZFHX3, ZFP1, ZFPM1, ZNF276, ZNF469, ZNF778, ZNRF1 studied for carcinoma

Included ClinVar conditions (242):
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 16q22.2-24.3(chr16:72107834-90142285)x1

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