Annotation Detail
Information
- Associated Genes
- ACO1 PLIN2 NUDT2 AQP3 AQP7 BAG1 CA9 CD72 CDKN2A CDKN2B CNTFR DMRT1 ELAVL2 FANCG MLANA GALT B4GALT1 GLDC DNAJA1 IFNA1 IFNA2 IFNA4 IFNA5 IFNA6 IFNA7 IFNA8 IFNA10 IFNA13 IFNA14 IFNA16 IFNA17 IFNA21 IFNB1 IFNW1 IL11RA INSL4 JAK2 MLLT3 MTAP NDUFB6 NFIB NFX1 NPR2 PRSS3 PTPRD RFX3 RLN1 RLN2 RMRP RPS6 CCL19 CCL21 SH3GL2 SLC1A1 SMARCA2 SNAPC3 TEK TESK1 TLN1 TPM2 TYRP1 VCP VLDLR MPDZ CER1 PLAA RGP1 RUSC2 PUM3 RCL1 TOPORS SIGMAR1 CREB3 UNC13B DMRT2 RRAGA CCL27 PSIP1 INSL6 DCTN3 KDM4C KANK1 PHF24 RIGI SLC24A2 DNAJB5 DCAF12 SPAG8 RANBP6 DNAI1 SIT1 SPINK4 CD274 STOML2 AK3 UBAP1 CHMP5 TMEM8B EQTN BNC2 HAUS6 APTX CNTLN FOCAD UBE2R2 SPATA6L SMU1 CDC37L1 DENND4C UBAP2 PLGRKT KLHL9 MYORG RIC1 GBA2 DMRT3 DMRTA1 LRRC19 NOL6 MOB3B CAAP1 ERMP1 IFT74 ATOSB PDCD1LG2 DOCK8 HINT2 SPMIP6 PIGO ARHGEF39 TPD52L3 IL33 DMAC1 ADAMTSL1 UHRF2 TAF1L ARID3C RPP25L SPATA31G1 DOCK8-AS1 LINGO2 TTC39B SAXO1 FREM1 BRD10 KCNV2 GLIS3 C9orf72 CCDC171 FAM219A CCDC107 SPATA31F1 TUSC1 LURAP1L IFNE ZDHHC21 ACER2 KIF24 ENHO FAM221B OR13J1 HACD4 TMEM215 PLPP6 MIR101-2 MIR31 ANKRD18B MSMP CIMIP2B CDKN2B-AS1 IZUMO3
- Associated Variants
- GRCh37/hg19 9p24.3-13.3(chr9:203861-35903398)x3
- Associated Disease
- MISSED ABORTION
- Source Database
- ClinVar
- Description
- GRCh37/hg19 9p24.3-13.3(chr9:203861-35903398)x3 AND MISSED ABORTION
- ClinVar Allele ID
- 1699179
- Clinical Significance Description
- Pathogenic
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002282974
- ClinVar Disease
- MISSED ABORTION
- Observed Origin Sample
- unknown
Drugs