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SNP Report
| Name | rs1601012 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr12:51685722 - 51685722(1) | ||
| Variant Alleles | A/C | ||
| Ancestral Allele | A | ||
| Minor Allele | A | ||
| Minor Allele Frequence | 0.356829 | ||
| Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000354534, ENST00000355133, ENST00000545061, ENST00000550891, ENST00000599343, ENST00000627620, ENST00000637709); NMD_transcript_variant(ENST00000637709); non_coding_transcript_variant(ENST00000550891); upstream_gene_variant(ENST00000551216) | ||
| No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | NO | ||
| Overlap with MDD? | NO | ||
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.



