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SNP Report
Name | rs2302659 dbSNP Ensembl | ||
---|---|---|---|
Location | chr2:170843849 - 170843849(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.207268 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000344257, ENST00000375272); intron_variant(ENST00000358196, ENST00000414527, ENST00000429023, ENST00000493875, ENST00000625689); NMD_transcript_variant(ENST00000414527, ENST00000493875); non_coding_transcript_exon_variant(ENST00000462739); non_coding_transcript_variant(ENST00000429023, ENST00000462739) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |