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- Data Summary
SNP Report
Basic Info
| Name | rs7290448 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr22:19915939(Fwd) | ||
| Variant Alleles | G/A | ||
| Ancestral Allele | G | ||
| Functional Annotation | intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000474308; ENST00000400525; ENST00000400521; ENST00000400519; ENST00000400518; ENST00000496729; ENST00000542719; ENST00000334363; ENST00000535882; ENST00000491939) nc_transcript_variant(ENST00000474308; ENST00000496729; ENST00000491939) |
||
| 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: 0)
Genes from other sources 
(count: 1)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.