SNP Report

Basic Info
| Name |
rs1984895
dbSNP
Ensembl
|
| Location |
chr1:231826551 - 231826551(1) |
| Variant Alleles |
G/A |
| Ancestral Allele |
G |
| Minor Allele |
A |
| Minor Allele Frequence |
0.251198 |
| Functional Annotation |
intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
|
| Consequence to Transcript |
intron_variant(ENST00000366632, ENST00000366633, ENST00000366636, ENST00000366637, ENST00000422590, ENST00000427560, ENST00000439617, ENST00000535983, ENST00000537876, ENST00000602713, ENST00000620189, ENST00000622252, ENST00000628350); NMD_transcript_variant(ENST00000366632, ENST00000422590, ENST00000602713); non_coding_transcript_variant(ENST00000427560) |
| No. of Studies |
1 (Positive: 0; Negative: 1; Trend: 0) |
| Source |
Literature |
| Overlap with SZ? |
YES
|
| Overlap with MDD? |
NO
|

SNP related studies (count: 1)

SNP related genes (count: 2)

Overlap with SZ from cross-disorder studies (count: 1)
| Reference |
Statistical Result |
Description |
Result Category |
| Thomson, P. A.,2005(a) |
Single-Marker Analysis:allele frequency, for SZ, P-value = 0.95 |
No significant association was observed. |
Negative |

Overlap with MDD from cross-disorder studies (count: 0)