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            SNP Report
| Name | rs303810 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr12:51769464 - 51769464(1) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | A | ||
| Minor Allele | A | ||
| Minor Allele Frequence | 0.321486 | ||
| Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000550891); intron_variant(ENST00000354534, ENST00000355133, ENST00000545061, ENST00000599343, ENST00000627620, ENST00000627665, ENST00000636945, ENST00000637709); NMD_transcript_variant(ENST00000636945, ENST00000637709); non_coding_transcript_variant(ENST00000627665); upstream_gene_variant(ENST00000548086, ENST00000636458) | ||
| No. of Studies | 1 (Positive: 1; Negative: 0; 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.



