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SNP Report
Name | rs11622475 dbSNP Ensembl | ||
---|---|---|---|
Location | chr14:104042739 - 104042739(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.248203 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000339063, ENST00000409874, ENST00000557332) | ||
No. of Studies | 4 (Positive: 0; Negative: 1; Trend: 3) | ||
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.