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SNP Report
| Name | rs2854248 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr1:160124137 - 160124137(1) | ||
| Variant Alleles | T/A | ||
| Ancestral Allele | T | ||
| Minor Allele | A | ||
| Minor Allele Frequence | 0.407149 | ||
| Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000478587); intron_variant(ENST00000361216, ENST00000392233, ENST00000468587, ENST00000472488, LRG_6t1); non_coding_transcript_variant(ENST00000468587, ENST00000472488); upstream_gene_variant(ENST00000447527) | ||
| No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | NO | ||
| Overlap with MDD? | NO | ||


