
Search SNP
Search Gene
Search CNV
Search Haplotype
Search Other Variant
Search Region
Search Pathway
Search Study
SNP Report
Name | rs816363 dbSNP Ensembl | ||
---|---|---|---|
Location | chr12:117222662 - 117222662(1) | ||
Variant Alleles | C/G | ||
Ancestral Allele | G | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.456669 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000317775, ENST00000338101, ENST00000344089, ENST00000618760) | ||
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.