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SNP Report
| Name | rs4078337 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr18:9138247 - 9138247(1) | ||
| Variant Alleles | T/G | ||
| Ancestral Allele | T | ||
| Minor Allele | T | ||
| Minor Allele Frequence | 0.403754 | ||
| Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000318388, ENST00000400033, ENST00000465096, ENST00000474740); intron_variant(ENST00000262126, ENST00000400020, ENST00000540578, ENST00000577992, ENST00000578850, ENST00000579126, ENST00000581635, ENST00000585234); NMD_transcript_variant(ENST00000581635); non_coding_transcript_variant(ENST00000540578, ENST00000578850, ENST00000579126); upstream_gene_variant(ENST00000582375, ENST00000583081, ENST00000608008) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


