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SNP Report
Name | rs9324684 dbSNP Ensembl | ||
---|---|---|---|
Location | chr5:151209052 - 151209052(1) | ||
Variant Alleles | G/C | ||
Ancestral Allele | C | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.387181 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000355417, ENST00000521308, ENST00000522179); non_coding_transcript_variant(ENST00000521308, ENST00000522179); upstream_gene_variant(ENST00000518189, ENST00000522964, ENST00000523466, ENST00000524344) | ||
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.