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SNP Report
Name | rs10038294 dbSNP Ensembl | ||
---|---|---|---|
Location | chr5:36913976 - 36913976(1) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Minor Allele | G | ||
Minor Allele Frequence | 0.034345 | ||
Functional Annotation | intron_variant. | ||
Consequence to Transcript | intron_variant(ENST00000282516, ENST00000448238, ENST00000621733) | ||
No. of Studies | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |