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SNP Report
| Name | rs6502097 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr17:82328303 - 82328303(1) | ||
| Variant Alleles | C/G | ||
| Ancestral Allele | G | ||
| Minor Allele | C | ||
| Minor Allele Frequence | 0.16893 | ||
| Functional Annotation | 5_prime_UTR_variant; intron_variant; NMD_transcript_variant. | ||
| Consequence to Transcript | 5_prime_UTR_variant(ENST00000581954); intron_variant(ENST00000269389, ENST00000580437, ENST00000581691, ENST00000581864, ENST00000582290, ENST00000582563, ENST00000583093); NMD_transcript_variant(ENST00000581864) | ||
| No. of Studies | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | YES | ||
| Overlap with MDD? | YES | ||
| Reference | Statistical Result | Description | Result Category |
|---|---|---|---|
| Matsunaga, S.,2012 | Chi square test:MAF = 0.16,P-value = 0.15,OR = 1.13 | No significant association was observed. | Negative |
| Reference | Statistical Result | Description | Result Category |
|---|---|---|---|
| Matsunaga, S.,2012 | Chi square test:MAF = 0.14,P-value = 0.48,OR = 0.92 | No significant association was observed. | Negative |


