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SNP Report
Name | rs149826123 dbSNP Ensembl | ||
---|---|---|---|
Location | chr17:3292483 - 3292483(1) | ||
Variant Alleles | A/G/T | ||
Minor Allele | T | ||
Minor Allele Frequence | 0.00179712 | ||
Functional Annotation | intron_variant; missense_variant; non_coding_transcript_variant.
Polyphen Annotation: possibly damaging(ENST00000323404' target='_blank'>ENST00000323404, ENST00000615105' target='_blank'>ENST00000615105); benign(ENST00000323404' target='_blank'>ENST00000323404, ENST00000615105' target='_blank'>ENST00000615105) SIFT Annotation: deleterious(ENST00000323404, ENST00000615105) |
||
Consequence to Transcript | intron_variant(ENST00000573491, ENST00000573901, ENST00000576166); missense_variant(ENST00000323404, ENST00000615105, ENST00000323404, ENST00000615105); non_coding_transcript_variant(ENST00000573491, ENST00000573901, ENST00000576166) | ||
No. of Studies | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature | ||
Overlap with SZ? | NO | ||
Overlap with MDD? | NO |