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SNP Report
Name | rs2273502 dbSNP Ensembl | ||
---|---|---|---|
Location | chr20:63356470 - 63356470(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.116414 | ||
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(ENST00000626188, ENST00000628606, ENST00000636726, ENST00000637443); intron_variant(ENST00000370263, ENST00000463705, ENST00000467563, ENST00000498043, ENST00000615287, ENST00000627000, ENST00000628665); NMD_transcript_variant(ENST00000498043, ENST00000627000); non_coding_transcript_exon_variant(ENST00000636481); non_coding_transcript_variant(ENST00000463705, ENST00000467563, ENST00000628665, ENST00000636481); upstream_gene_variant(ENST00000370257, ENST00000627869, ENST00000636652, ENST00000637243, ENST00000637628) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |