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SNP Report
| Name | rs4148965 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr18:9109486 - 9109486(1) | ||
| Variant Alleles | T/G | ||
| Ancestral Allele | T | ||
| Minor Allele | T | ||
| Minor Allele Frequence | 0.360423 | ||
| Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000579467); intron_variant(ENST00000318388, ENST00000400033, ENST00000577703, ENST00000578850, ENST00000579126, ENST00000583375); NMD_transcript_variant(ENST00000577703); non_coding_transcript_variant(ENST00000578850, ENST00000579126, ENST00000583375) | ||
| 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.



