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SNP Report
Name | rs7839852 dbSNP Ensembl | ||
---|---|---|---|
Location | chr8:28848548 - 28848548(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.234425 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000520831); intron_variant(ENST00000416984, ENST00000518510, ENST00000520184, ENST00000520437, ENST00000520983, ENST00000521022, ENST00000521777, ENST00000522363, ENST00000523303, ENST00000523436, ENST00000524081); NMD_transcript_variant(ENST00000518510, ENST00000520437, ENST00000522363, ENST00000523303); non_coding_transcript_variant(ENST00000520983) | ||
No. of Studies | 1 (Positive: 1; Negative: 0; 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.