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SNP Report
Name | rs3735568 dbSNP Ensembl | ||
---|---|---|---|
Location | chr7:28176035 - 28176035(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.311302 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000283928, ENST00000452993, ENST00000454041); NMD_transcript_variant(ENST00000452993, ENST00000454041); upstream_gene_variant(ENST00000436758, ENST00000455963) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |