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SNP Report
Name | rs10982256 dbSNP Ensembl | ||
---|---|---|---|
Location | chr9:114498554 - 114498554(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.38758 | ||
Functional Annotation | downstream_gene_variant; intron_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000480518); intron_variant(ENST00000265134, ENST00000362057, ENST00000374057) | ||
No. of Studies | 3 (Positive: 1; Negative: 0; 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.