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SNP Report
Name | rs17350383 dbSNP Ensembl | ||
---|---|---|---|
Location | chr7:18890590 - 18890590(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.134784 | ||
Functional Annotation | downstream_gene_variant; intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000447057); intron_variant(ENST00000401921, ENST00000406451, ENST00000432645, ENST00000441542, ENST00000483142, ENST00000490851, ENST00000496026); non_coding_transcript_variant(ENST00000483142, ENST00000490851, ENST00000496026) | ||
No. of Studies | 1 (Positive: 0; 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.