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SNP Report
Name | rs34058821 dbSNP Ensembl | ||
---|---|---|---|
Location | chr4:7664433 - 7664433(1) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.0195687 | ||
Functional Annotation | downstream_gene_variant; missense_variant.
Polyphen Annotation: possibly damaging(ENST00000329016, ENST00000507866) SIFT Annotation: tolerated(ENST00000329016, ENST00000507866) |
||
Consequence to Transcript | downstream_gene_variant(ENST00000511199); missense_variant(ENST00000329016, ENST00000507866) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |