SNP Report

Basic Info
Name |
rs2303377
dbSNP
Ensembl
|
Location |
chr11:113240779 - 113240779(1) |
Variant Alleles |
T/C |
Ancestral Allele |
T |
Minor Allele |
C |
Minor Allele Frequence |
0.413938 |
Functional Annotation |
intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; splice_region_variant.
|
Consequence to Transcript |
intron_variant(ENST00000316851, ENST00000401611, ENST00000525355, ENST00000526322, ENST00000528590, ENST00000530543, ENST00000531044, ENST00000531817, ENST00000533073, ENST00000611284, ENST00000615112, ENST00000615285, ENST00000618266, ENST00000619839, ENST00000620046, ENST00000621128, ENST00000621518, ENST00000621850); NMD_transcript_variant(ENST00000531817); non_coding_transcript_exon_variant(ENST00000525691); non_coding_transcript_variant(ENST00000525355, ENST00000525691, ENST00000611284); splice_region_variant(ENST00000526322, ENST00000528590, ENST00000531817, ENST00000621518, ENST00000621850) |
No. of Studies |
1 (Positive: 1; Negative: 0; Trend: 0) |
Source |
Literature |
Overlap with SZ? |
YES
|
Overlap with MDD? |
NO
|

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 |
Atz, M. E., 2007 |
Fisher's exact test, allelic P-value = 0.24 in SZ; Fisher's exact test, allelic P-value = 0.264 in BD&SZ |
SNP b was not associated with SZ. |
Negative |

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