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SNP Report
| Name | rs4430518 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr11:120852724 - 120852724(1) | ||
| Variant Alleles | T/G | ||
| Ancestral Allele | T | ||
| Minor Allele | G | ||
| Minor Allele Frequence | 0.32488 | ||
| 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: 0; Negative: 1; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | YES | ||
| Overlap with MDD? | NO | ||
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.
| Reference | Statistical Result | Description | Result Category |
|---|---|---|---|
| Pickard, B. S., 2006 | P-value = 0.015 between SCZ cases and controls; P-value = 0.244 between all cases and controls | showed significant association with schizophrenia | Positive |



