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SNP Report
Name | rs34116 dbSNP Ensembl | ||
---|---|---|---|
Location | chr5:81146180 - 81146180(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.344649 | ||
Functional Annotation | intron_variant; NMD_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000265080, ENST00000503795); NMD_transcript_variant(ENST00000503795) | ||
No. of Studies | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |