Search SNP
Search Gene
Search CNV
Search Haplotype
Search Other Variant
Search Region
Search Pathway
Search Study
SNP Report
| Name | rs1005173 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr21:44415083 - 44415083(1) | ||
| Variant Alleles | G/A/C/T | ||
| Ancestral Allele | G | ||
| Minor Allele | G | ||
| Minor Allele Frequence | 0.330871 | ||
| Functional Annotation | intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000300481, ENST00000300482, ENST00000397928, ENST00000397932, ENST00000423310, ENST00000498430); non_coding_transcript_exon_variant(ENST00000456880); non_coding_transcript_variant(ENST00000423310, ENST00000456880, ENST00000498430) | ||
| No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


