Search SNP
Search Gene
Search CNV
Search Haplotype
Search Other Variant
Search Region
Search Pathway
Search Study
SNP Report
Name | rs4786120 dbSNP Ensembl | ||
---|---|---|---|
Location | chr16:6753551 - 6753551(1) | ||
Variant Alleles | G/C | ||
Ancestral Allele | G | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.169928 | ||
Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000516271); intron_variant(ENST00000422070, ENST00000535565, ENST00000547372, ENST00000547427, ENST00000547605, ENST00000550418, ENST00000551752, ENST00000552089, ENST00000553186, ENST00000569895); non_coding_transcript_variant(ENST00000547427, ENST00000569895) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |