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SNP Report
Basic Info
| Name | rs38478 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr7:30561338 - 30561338(1) | ||
| Variant Alleles | G/A | ||
| Ancestral Allele | G | ||
| Minor Allele | G | ||
| Minor Allele Frequence | 0.262979 | ||
| Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000582145, ENST00000584108, ENST00000584199, ENST00000614950, ENST00000621272); intron_variant(ENST00000426529, ENST00000434399, ENST00000577889, ENST00000578245, ENST00000578293, ENST00000578572, ENST00000580902, ENST00000584621, ENST00000626902, ENST00000631229); non_coding_transcript_exon_variant(ENST00000355837); non_coding_transcript_variant(ENST00000355837, ENST00000426529, ENST00000434399, ENST00000577889, ENST00000578245, ENST00000578293, ENST00000578572, ENST00000580902, ENST00000584621, ENST00000626902, ENST00000631229) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 0)
Overlap with SZ from cross-disorder studies (count: 0)
Overlap with MDD from cross-disorder studies (count: 0)