Annotation Detail
Information
- Associated Genes
- FGFR1 ADAM2 IDO1 TACC1 ADAM18 ADAM9 NSD3 TCIM PLEKHA2 ZMAT4 TM2D2 LETM2 IDO2 HTRA4 ADAM32 LINC03042 LOC100130964 LOC102723716 LOC105379385 LINC02866 LOC107133509 SNORD38D LOC111413020 LOC111500313 SIRLNT LOC113788279 LOC113788280 LOC121331299 LOC124153147 LOC124153148 LOC124153149 LOC124153150 LOC124153151 LOC124153152 LOC124153153 LOC126860361 LOC126860362 LOC126860363 LOC126860364 LOC130000225 LOC130000226 LOC130000227 LOC130000228 LOC130000229 LOC130000230 LOC130000231 LOC130000232 LOC130000233 LOC130000234 LOC130000235 LOC130000236 LOC130000237 LOC130000238 LOC130000239 LOC130000240 LOC130000241 LOC130000242 LOC130000243 LOC130000244 LOC130000245 LOC130000246 LOC130000247 LOC130000248 LOC130000249 LOC130000250 LOC130000251 LOC130000252 LOC130000253 LOC130000254 LOC130000255 LOC130000256 LOC130000257 LOC130000258 LOC130000259 LOC130000260 LOC130000261 LOC130000262 LOC130000263 LOC130000264 LOC130000265 LOC130000266 LOC130000267 LOC130000268
- Associated Variants
-
GRCh38/hg38 8p11.23-11.21(chr8:38342177-40546982)x1
GRCh38/hg38 8p11.23-11.21(chr8:38342177-40546982)x1 - Source Database
- ClinVar
- Description
- GRCh38/hg38 8p11.23-11.21(chr8:38342177-40546982)x1 AND See cases
- ClinVar Allele ID
- 74955
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2011-08-12
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000054238
- Observed Origin Sample
- not provided
Drugs