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SNP Report
Name | rs733457 dbSNP Ensembl | ||
---|---|---|---|
Location | chr6:34100631 - 34100631(1) | ||
Variant Alleles | G/A/T | ||
Ancestral Allele | T | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.40016 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000374177, ENST00000374181, ENST00000455714, ENST00000535756, ENST00000538487, ENST00000544773, ENST00000607916, ENST00000609222, ENST00000609278, ENST00000609973); NMD_transcript_variant(ENST00000609278); non_coding_transcript_variant(ENST00000607916, ENST00000609973); upstream_gene_variant(ENST00000609443) | ||
No. of Studies | 2 (Positive: 1; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.