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SNP Report
Name | rs9503522 dbSNP Ensembl | ||
---|---|---|---|
Location | chr6:3284686 - 3284686(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.296326 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000467144); intron_variant(ENST00000380302, ENST00000406686, ENST00000436008, ENST00000451246, ENST00000454610, ENST00000467177, ENST00000485307, ENST00000490273, ENST00000497691); NMD_transcript_variant(ENST00000497691); upstream_gene_variant(ENST00000482874) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |