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- Data Summary
SNP Report
Basic Info
| Name | rs1018124 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr2:234676118(Fwd) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | A | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000450233; ENST00000446481) downstream_gene_variant(ENST00000484784) intron_variant(ENST00000373426; ENST00000373445; ENST00000373450; ENST00000373424; ENST00000344644; ENST00000354728; ENST00000373414; ENST00000360418; ENST00000482026; ENST00000305208; ENST00000305139; ENST00000373409; ENST00000450233; ENST00000406651; ENST00000446481) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 9)
Literature-origin genes (count: 1)
Genes from other sources 
(count: 8)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.