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SNP Report
Name | rs593713 dbSNP Ensembl | ||
---|---|---|---|
Location | chr18:11887658 - 11887658(1) | ||
Variant Alleles | G/A | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.496206 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000334049, ENST00000586364, ENST00000588186, ENST00000588191, ENST00000589267); intron_variant(ENST00000309976, ENST00000317235, ENST00000317251, ENST00000344987, ENST00000496196, ENST00000587724, ENST00000588072, ENST00000589731, ENST00000592331, ENST00000592447, ENST00000592894, ENST00000592977); NMD_transcript_variant(ENST00000317251, ENST00000496196); non_coding_transcript_variant(ENST00000589731, ENST00000592447, ENST00000592894); upstream_gene_variant(ENST00000592306, ENST00000592755) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |