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SNP Report
Name | rs10102186 dbSNP Ensembl | ||
---|---|---|---|
Location | chr8:26767134 - 26767134(1) | ||
Variant Alleles | G/A | ||
Minor Allele | A | ||
Minor Allele Frequence | 0.246406 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000276393, ENST00000380573, ENST00000518621); intron_variant(ENST00000354550, ENST00000380582, ENST00000380586, ENST00000519096, ENST00000519229, ENST00000521711); NMD_transcript_variant(ENST00000519096, ENST00000521711); upstream_gene_variant(ENST00000486251) | ||
No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |