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SNP Report
| Name | rs762967 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr22:35344873 - 35344873(1) | ||
| Variant Alleles | G/A | ||
| Ancestral Allele | G | ||
| Minor Allele | A | ||
| Minor Allele Frequence | 0.0439297 | ||
| Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000382034, ENST00000404284, ENST00000411850, ENST00000424387, ENST00000425375, ENST00000447733, ENST00000449058); NMD_transcript_variant(ENST00000404284, ENST00000424387); non_coding_transcript_exon_variant(ENST00000492723); non_coding_transcript_variant(ENST00000492723) | ||
| No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | NO | ||
| Overlap with MDD? | NO | ||


