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SNP Report
Name | rs10482616 dbSNP Ensembl | ||
---|---|---|---|
Location | chr5:143402002 - 143402002(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.193291 | ||
Functional Annotation | intron_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000231509, ENST00000343796, ENST00000394464, ENST00000394466, ENST00000415690, ENST00000502892, ENST00000503201, ENST00000504572, ENST00000508760, ENST00000510170, ENST00000514699); upstream_gene_variant(ENST00000424646, ENST00000502500, ENST00000623204) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |