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SNP Report
Name | rs9322993 dbSNP Ensembl | ||
---|---|---|---|
Location | chr14:39136338 - 39136338(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.176518 | ||
Functional Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000524781, ENST00000529365, ENST00000531684, ENST00000534684); intron_variant(ENST00000250379, ENST00000308317, ENST00000396249, ENST00000412033, ENST00000524980, ENST00000525153); NMD_transcript_variant(ENST00000412033, ENST00000525153); non_coding_transcript_variant(ENST00000524980) | ||
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.