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SNP Report
Name | rs11171856 dbSNP Ensembl | ||
---|---|---|---|
Location | chr12:56448035 - 56448035(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.368411 | ||
Functional Annotation | downstream_gene_variant; intron_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000257979, ENST00000555551); intron_variant(ENST00000229201, ENST00000553532) | ||
No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |