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SNP Report
Name | rs2839223 dbSNP Ensembl | ||
---|---|---|---|
Location | chr21:46357148 - 46357148(1) | ||
Variant Alleles | G/A | ||
Ancestral Allele | A | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.151358 | ||
Functional Annotation | downstream_gene_variant; missense_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Polyphen Annotation: benign(ENST00000359568) SIFT Annotation: tolerated(ENST00000359568) |
||
Consequence to Transcript | downstream_gene_variant(ENST00000466474, ENST00000483844); missense_variant(ENST00000359568); non_coding_transcript_exon_variant(ENST00000480896); non_coding_transcript_variant(ENST00000480896) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |