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SNP Report
Name | rs4276227 dbSNP Ensembl | ||
---|---|---|---|
Location | chr3:32289194 - 32289194(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | T | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.33107 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000307526, ENST00000458535) | ||
No. of Studies | 3 (Positive: 0; Negative: 1; Trend: 2) | ||
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.