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SNP Report
Name | rs673735 dbSNP Ensembl | ||
---|---|---|---|
Location | chr18:11893392 - 11893392(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.238019 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000586844, ENST00000587381, ENST00000588103, ENST00000589829, ENST00000589859, ENST00000590501, ENST00000591667, ENST00000593001); intron_variant(ENST00000309976, ENST00000317235, ENST00000317251, ENST00000344987, ENST00000496196, ENST00000586364, ENST00000588072, ENST00000588186, ENST00000588191, ENST00000589267, ENST00000589731, ENST00000592331, ENST00000592447, ENST00000592894, ENST00000592977); NMD_transcript_variant(ENST00000317251, ENST00000496196); non_coding_transcript_exon_variant(ENST00000592180); non_coding_transcript_variant(ENST00000586364, ENST00000589731, ENST00000592180, ENST00000592447, ENST00000592894); upstream_gene_variant(ENST00000587724) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |