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- Data Summary
SNP Report
Basic Info
| Name | rs2073157 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr6:41655005(Fwd) | ||
| Variant Alleles | G/A | ||
| Ancestral Allele | A | ||
| Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000425401; ENST00000445214; ENST00000419788; ENST00000419574; ENST00000424495; ENST00000445700; ENST00000433032; ENST00000597468) intron_variant(ENST00000358871; ENST00000394283; ENST00000406563; ENST00000373033; ENST00000416140; ENST00000230323; ENST00000343317; ENST00000494822; ENST00000419396; ENST00000420312; ENST00000403298) nc_transcript_variant(ENST00000494822) |
||
| 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.