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SNP Report
Name | rs11065501 dbSNP Ensembl | ||
---|---|---|---|
Location | chr12:121234167 - 121234167(1) | ||
Variant Alleles | C/G | ||
Ancestral Allele | C | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.241214 | ||
Functional Annotation | downstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000324774, ENST00000337174, ENST00000337233, ENST00000347034, ENST00000359949, ENST00000392474, ENST00000499638, ENST00000538417, ENST00000538733, ENST00000541187, ENST00000542067, ENST00000543171, ENST00000543318, ENST00000543430, ENST00000543984, ENST00000545538) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; 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.