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SNP Report
Name | rs2301622 dbSNP Ensembl | ||
---|---|---|---|
Location | chr12:111457399 - 111457399(1) | ||
Variant Alleles | C/G | ||
Ancestral Allele | G | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.464657 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000377617, ENST00000389153, ENST00000389154, ENST00000482777, ENST00000483311, ENST00000535949, ENST00000542287, ENST00000550104, ENST00000550844, ENST00000550889, ENST00000608853, ENST00000616825); NMD_transcript_variant(ENST00000483311); non_coding_transcript_exon_variant(ENST00000468920, ENST00000551551); non_coding_transcript_variant(ENST00000468920, ENST00000482777, ENST00000550889, ENST00000551551); upstream_gene_variant(ENST00000475132, ENST00000484991) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |