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SNP Report
Name | rs12454936 dbSNP Ensembl | ||
---|---|---|---|
Location | chr18:9134440 - 9134440(1) | ||
Variant Alleles | C/G | ||
Ancestral Allele | C | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.0752796 | ||
Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000318388, ENST00000400033, ENST00000465096, ENST00000474740, ENST00000608008); intron_variant(ENST00000578850, ENST00000579126, ENST00000582375); non_coding_transcript_variant(ENST00000578850, ENST00000579126, ENST00000582375); upstream_gene_variant(ENST00000262126, ENST00000400020, ENST00000540578, ENST00000577992, ENST00000581635, ENST00000583081, ENST00000585234) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |