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SNP Report
Name | rs452223 dbSNP Ensembl | ||
---|---|---|---|
Location | chr5:157184482 - 157184482(1) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.263778 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000422843, ENST00000517779, ENST00000519402, ENST00000520555, ENST00000521769, ENST00000522616, LRG_189t1); NMD_transcript_variant(ENST00000517779); non_coding_transcript_variant(ENST00000519402, ENST00000520555, ENST00000522616) | ||
No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |