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SNP Report
Name | rs4412625 dbSNP Ensembl |
---|---|
Location | chrCHR_HSCHR1_3_CTG31:198392289 - 198392289(1) |
Variant Alleles | G/T |
Ancestral Allele | T |
Minor Allele | G |
Minor Allele Frequence | 0.304912 |
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.