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SNP Report
Name | rs129962 dbSNP Ensembl | ||
---|---|---|---|
Location | chr16:3745725 - 3745725(1) | ||
Variant Alleles | A/T | ||
Ancestral Allele | T | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.209864 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000262367, ENST00000382070, ENST00000570939, ENST00000573517, ENST00000638158); non_coding_transcript_variant(ENST00000638158); upstream_gene_variant(ENST00000572569, ENST00000574740, ENST00000576720, ENST00000635919) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |