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SNP Report
| Name | rs4444432 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr19:58204171 - 58204171(1) | ||
| Variant Alleles | T/G | ||
| Ancestral Allele | G | ||
| Minor Allele | G | ||
| Minor Allele Frequence | 0.117812 | ||
| Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000601995); intron_variant(ENST00000326804, ENST00000345813, ENST00000424679, ENST00000594839, ENST00000610905, ENST00000615675, ENST00000617501, ENST00000619307, ENST00000621145); non_coding_transcript_variant(ENST00000615675, ENST00000619307, ENST00000621145); upstream_gene_variant(ENST00000595146) | ||
| 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.



