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SNP Report
| Name | rs17153639 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr7:26443506 - 26443506(1) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Minor Allele | T | ||
| Minor Allele Frequence | 0.034345 | ||
| Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000421862, ENST00000430548, ENST00000439120, ENST00000448056); non_coding_transcript_variant(ENST00000421862, ENST00000430548, ENST00000439120, ENST00000448056) | ||
| No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | NO | ||
| Overlap with MDD? | NO | ||


