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SNP Report
Name | rs6597678 dbSNP Ensembl | ||
---|---|---|---|
Location | chr9:131149084 - 131149084(1) | ||
Variant Alleles | G/C | ||
Ancestral Allele | G | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.0181709 | ||
Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000530863); intron_variant(ENST00000359428, ENST00000411637, ENST00000415391, ENST00000451030, ENST00000525980, ENST00000586290, ENST00000587264, ENST00000587408, ENST00000588378, ENST00000589540, ENST00000589667, ENST00000590461); non_coding_transcript_variant(ENST00000415391, ENST00000525980, ENST00000586290, ENST00000587264, ENST00000587408, ENST00000588378, ENST00000589540, ENST00000589667, ENST00000590461); upstream_gene_variant(ENST00000530630) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |