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SNP Report
Name | rs224277 dbSNP Ensembl | ||
---|---|---|---|
Location | chr10:62820301 - 62820301(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.411542 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000493899); non_coding_transcript_variant(ENST00000493899); upstream_gene_variant(ENST00000242480, ENST00000411732, ENST00000439032, ENST00000637191, LRG_239t1) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |