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SNP Report
| Name | rs4494918 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr3:51649232 - 51649232(1) | ||
| Variant Alleles | G/C | ||
| Ancestral Allele | G | ||
| Minor Allele | G | ||
| Minor Allele Frequence | 0.293331 | ||
| Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000409535, ENST00000432863, ENST00000461680, ENST00000487093); non_coding_transcript_variant(ENST00000461680, ENST00000487093) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


