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SNP Report
Name | rs748856 dbSNP Ensembl | ||
---|---|---|---|
Location | chr8:122802586 - 122802586(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.497005 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000314393) | ||
No. of Studies | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |