
Search SNP
Search Gene
Search CNV
Search Haplotype
Search Other Variant
Search Region
Search Pathway
Search Study
SNP Report
Name | rs169068 dbSNP Ensembl | ||
---|---|---|---|
Location | chr16:1079872 - 1079872(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.481829 | ||
Functional Annotation | missense_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000293897) SIFT Annotation: tolerated(ENST00000293897) |
||
Consequence to Transcript | missense_variant(ENST00000293897); upstream_gene_variant(ENST00000566499, ENST00000569832, ENST00000624643) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |