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SNP Report
| Name | rs12154715 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr7:158935219 - 158935219(1) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | A | ||
| Minor Allele | G | ||
| Minor Allele Frequence | 0.120407 | ||
| Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000407559, ENST00000444851, ENST00000454771, ENST00000467220); NMD_transcript_variant(ENST00000444851, ENST00000454771); non_coding_transcript_variant(ENST00000467220) | ||
| No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | NO | ||
| Overlap with MDD? | NO | ||
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.



