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SNP Report
Name | rs2007211 dbSNP Ensembl | ||
---|---|---|---|
Location | chr11:111859227 - 111859227(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.326278 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000398006, ENST00000530851, ENST00000531154, ENST00000612489, ENST00000613181, ENST00000614444, ENST00000616540, ENST00000618252, ENST00000619129, ENST00000622211); NMD_transcript_variant(ENST00000612489, ENST00000613181, ENST00000618252, ENST00000619129); non_coding_transcript_variant(ENST00000530851); upstream_gene_variant(ENST00000527714) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |