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SNP Report
| Name | rs4890047 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr17:80575639 - 80575639(1) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Minor Allele | T | ||
| Minor Allele Frequence | 0.35004 | ||
| Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000306801, ENST00000544334, ENST00000570891, ENST00000573746, ENST00000574767, ENST00000577161); NMD_transcript_variant(ENST00000574767); non_coding_transcript_variant(ENST00000573746, ENST00000577161) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


