
SNP Report
| Name | rs10835210 dbSNP Ensembl |
|---|---|
| Location | Chrchr11:27695910(Forward) |
| Variant Alleles | C/A |
| Ancestral Allele | C |
| Annotation | intron_variant; nc_transcript_variant; NMD_transcript_variant |
| Consequence to Transcript | intron_variant(ENST00000314915, ENST00000356660, ENST00000395978, ENST00000395980, ENST00000395981, ENST00000395983, ENST00000395986, ENST00000418212, ENST00000420794, ENST00000438929, ENST00000499008, ENST00000499568, ENST00000500662, ENST00000501176, ENST00000501663, ENST00000502161, ENST00000525950, ENST00000530686, ENST00000530786, ENST00000530861, ENST00000532997, ENST00000533131, ENST00000533246, ENST00000584049) nc_transcript_variant(ENST00000499008, ENST00000499568, ENST00000500662, ENST00000501176, ENST00000501663, ENST00000502161, ENST00000530686, ENST00000584049) NMD_transcript_variant(ENST00000530786) |
| No. of Studies (Positive/Negative) | 1 (0/1)
|

