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SNP Report
Name | rs2926835 dbSNP Ensembl | ||
---|---|---|---|
Location | chr5:153809370 - 153809370(1) | ||
Variant Alleles | T/A | ||
Ancestral Allele | T | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.407149 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000285900, ENST00000340592, ENST00000448073, ENST00000518142, ENST00000518783, ENST00000521843) | ||
No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.