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SNP Report
Name | rs6580038 dbSNP Ensembl | ||
---|---|---|---|
Location | chr5:153753281 - 153753281(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.28115 | ||
Functional Annotation | intron_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000285900, ENST00000340592, ENST00000448073, ENST00000518142, ENST00000518783, ENST00000521843); upstream_gene_variant(ENST00000476596) | ||
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.