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SNP Report
Name | rs220592 dbSNP Ensembl | ||
---|---|---|---|
Location | chr12:13812374 - 13812374(1) | ||
Variant Alleles | C/A | ||
Ancestral Allele | A | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.353634 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000609686) | ||
No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |