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SNP Report
| Name | rs2835265 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr21:36072398 - 36072398(1) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Minor Allele | T | ||
| Minor Allele Frequence | 0.126398 | ||
| Functional Annotation | 3_prime_UTR_variant; downstream_gene_variant; intron_variant; missense_variant; non_coding_transcript_variant.
Polyphen Annotation: unknown(ENST00000399191) |
||
| Consequence to Transcript | 3_prime_UTR_variant(ENST00000530908); downstream_gene_variant(ENST00000415147, ENST00000439427, ENST00000466328); intron_variant(ENST00000290349, ENST00000399201, ENST00000535199); missense_variant(ENST00000399191); non_coding_transcript_variant(ENST00000535199) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


