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SNP Report
Name | rs2271308 dbSNP Ensembl | ||
---|---|---|---|
Location | chr17:39661229 - 39661229(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.451078 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000443521, ENST00000460894, ENST00000484773, ENST00000577248, ENST00000578232, ENST00000578254, ENST00000579479, ENST00000580331, ENST00000580551, ENST00000581894, ENST00000582874, ENST00000583419, ENST00000583582, ENST00000583718, ENST00000585214); intron_variant(ENST00000336308, ENST00000394250, ENST00000471896, ENST00000481171, ENST00000488876, ENST00000544210, ENST00000578384, ENST00000578577, ENST00000580611, ENST00000583639, ENST00000583884, ENST00000584850, ENST00000585269); NMD_transcript_variant(ENST00000578577, ENST00000583884); non_coding_transcript_exon_variant(ENST00000578686); non_coding_transcript_variant(ENST00000471896, ENST00000481171, ENST00000488876, ENST00000578384, ENST00000578686, ENST00000583639, ENST00000584850, ENST00000585269); upstream_gene_variant(ENST00000309889, ENST00000578283, LRG_210t1) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |