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SNP Report
Name | rs1273394 dbSNP Ensembl | ||
---|---|---|---|
Location | chr16:8719430 - 8719430(1) | ||
Variant Alleles | G/T | ||
Ancestral Allele | T | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.284944 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000563215); intron_variant(ENST00000268251, ENST00000396600, ENST00000561870, ENST00000563992, ENST00000564714, ENST00000565016, ENST00000566590, ENST00000567812, ENST00000568847); NMD_transcript_variant(ENST00000566590); non_coding_transcript_variant(ENST00000563992); upstream_gene_variant(ENST00000425191, ENST00000562115, ENST00000569156) | ||
No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |