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SNP Report
Name | rs2242663 dbSNP Ensembl | ||
---|---|---|---|
Location | chr11:66567837 - 66567837(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.208267 | ||
Functional Annotation | downstream_gene_variant; intron_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000502692, ENST00000513398); intron_variant(ENST00000310325, ENST00000526010); upstream_gene_variant(ENST00000524994, ENST00000525733, ENST00000527141, ENST00000529199, ENST00000529561, ENST00000530565, ENST00000533168) | ||
No. of Studies | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |