SNP Report

Basic Info
Name |
rs688325
dbSNP
Ensembl
|
Location |
chr1:147605490 - 147605490(1) |
Variant Alleles |
G/A |
Ancestral Allele |
A |
Minor Allele |
A |
Minor Allele Frequence |
0.292532 |
Functional Annotation |
intron_variant; non_coding_transcript_variant.
|
Consequence to Transcript |
intron_variant(ENST00000234739, ENST00000497938); non_coding_transcript_variant(ENST00000497938) |
No. of Studies |
1 (Positive: 0; Negative: 1; Trend: 0) |
Source |
Literature |
Overlap with SZ? |
YES
|
Overlap with MDD? |
YES
|

SNP related studies (count: 1)

SNP related genes (count: 1)

Overlap with SZ from cross-disorder studies (count: 1)
Reference |
Statistical Result |
Description |
Result Category |
Li, J.,2011(b) |
Third-Stage Sample:for SZ, allele association P-value = 0.006, OR(95%CI)=1.19(1.05-1.33);Combined Third-Stage Sample, allele association P-value = 0.000254, OR(98%CI)=1.11(1.05-1.18) |
Significant association was observed in SZ. |
Positive |

Overlap with MDD from cross-disorder studies (count: 1)
Reference |
Statistical Result |
Description |
Result Category |
Li, J.,2011(b) |
Third-Stage Sample:for MDD, allele association P-value = 0.02, OR(95%CI)=1.16(1.03-1.32) |
Significant association was observed in MDD. |
Positive
|