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SNP Report
Name | rs6571917 dbSNP Ensembl | ||
---|---|---|---|
Location | chr14:39309695 - 39309695(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.0896565 | ||
Functional Annotation | intron_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000280083, ENST00000341502, ENST00000341749, ENST00000348007, ENST00000396158, ENST00000396165, ENST00000553352, ENST00000553728, ENST00000556148, ENST00000557038); upstream_gene_variant(ENST00000556593) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |