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- Data Summary
SNP Report
Basic Info
| Name | rs4238726 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr16:83117722(Fwd) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | C | ||
| Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000539548) intron_variant(ENST00000566620; ENST00000268613; ENST00000565636; ENST00000431540; ENST00000428848; ENST00000539548; ENST00000569454; ENST00000446376) nc_transcript_variant(ENST00000569454) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 1)
Literature-origin genes (count: 1)
Genes from other sources 
(count: 0)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.