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SNP Report
Name | rs683395 dbSNP Ensembl | ||
---|---|---|---|
Location | chr3:183152030 - 183152030(1) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.129593 | ||
Functional Annotation | downstream_gene_variant; intron_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000470251, ENST00000476015); intron_variant(ENST00000265598, ENST00000466939) | ||
No. of Studies | 3 (Positive: 0; Negative: 1; Trend: 2) | ||
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.