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SNP Report
Name | rs17153639 dbSNP Ensembl | ||
---|---|---|---|
Location | chr7:26443506 - 26443506(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.034345 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000421862, ENST00000430548, ENST00000439120, ENST00000448056); non_coding_transcript_variant(ENST00000421862, ENST00000430548, ENST00000439120, ENST00000448056) | ||
No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |