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SNP Report
Name | rs9554603 dbSNP Ensembl | ||
---|---|---|---|
Location | chr13:99494828 - 99494828(1) | ||
Variant Alleles | G/T | ||
Ancestral Allele | T | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.275359 | ||
Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000366259, ENST00000625254, ENST00000625369); intron_variant(ENST00000630421); non_coding_transcript_exon_variant(ENST00000626729); non_coding_transcript_variant(ENST00000626729, ENST00000630421); upstream_gene_variant(ENST00000625287, ENST00000626308, ENST00000627052) | ||
No. of Studies | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |