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SNP Report
Name | rs2156635 dbSNP Ensembl | ||
---|---|---|---|
Location | chr11:120900959 - 120900959(1) | ||
Variant Alleles | C/G | ||
Ancestral Allele | C | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.41274 | ||
Functional Annotation | intron_variant; non_coding_transcript_variant. | ||
Consequence to Transcript | intron_variant(ENST00000438375, ENST00000527524, ENST00000533291); non_coding_transcript_variant(ENST00000533291) | ||
No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature | ||
Overlap with SZ? | YES | ||
Overlap with MDD? | NO |
Reference | Statistical Result | Description | Result Category |
---|---|---|---|
Pickard, B. S., 2006 | P-value = 0.081 between SCZ cases and controls; P-value = 0.041 between all cases and controls | Positive |