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- Data Summary
SNP Report
Basic Info
| Name | rs10848642 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr12:2331572(Fwd) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | G | ||
| Functional Annotation | intron_variant; nc_transcript_variant; non_coding_exon_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000335762; ENST00000399655; ENST00000480911; ENST00000399595; ENST00000399644; ENST00000399638; ENST00000399597; ENST00000399621; ENST00000399637; ENST00000399591; ENST00000399641; ENST00000347598; ENST00000399606; ENST00000399601; ENST00000344100; ENST00000399629; ENST00000327702; ENST00000399649; ENST00000402845; ENST00000399617; ENST00000399634; ENST00000399603; ENST00000406454; LRG_334_t2; LRG_334_t4; LRG_334_t3; LRG_334_t1) nc_transcript_variant(ENST00000544415) non_coding_exon_variant(ENST00000544415) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 2)
Literature-origin genes (count: 1)
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.