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SNP Report
Name | rs145244580 dbSNP Ensembl | ||
---|---|---|---|
Location | chr7:93195875 - 93195875(1) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.00119808 | ||
Functional Annotation | missense_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; synonymous_variant.
Polyphen Annotation: probably damaging(ENST00000341723, ENST00000394468, ENST00000453812) SIFT Annotation: deleterious(ENST00000341723, ENST00000394468, ENST00000453812) |
||
Consequence to Transcript | missense_variant(ENST00000341723, ENST00000394468, ENST00000453812); non_coding_transcript_exon_variant(ENST00000492616); non_coding_transcript_variant(ENST00000492616); synonymous_variant(ENST00000440868) | ||
No. of Studies | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |