SNP Report

Basic Info
| Name |
rs2072621
dbSNP
Ensembl
|
| Location |
chrX:151177387 - 151177387(1) |
| Variant Alleles |
C/A |
| Ancestral Allele |
C |
| Minor Allele |
A |
| Minor Allele Frequence |
0.274702 |
| Functional Annotation |
intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
|
| Consequence to Transcript |
intron_variant(ENST00000218316); non_coding_transcript_exon_variant(ENST00000454196); non_coding_transcript_variant(ENST00000454196); upstream_gene_variant(ENST00000602313) |
| No. of Studies |
2 (Positive: 0; Negative: 2; Trend: 0) |
| Source |
Literature |
| Overlap with SZ? |
YES
|
| Overlap with MDD? |
YES
|

SNP related studies (count: 2)

SNP related genes (count: 2)

Overlap with SZ from cross-disorder studies (count: 1)
| Reference |
Statistical Result |
Description |
Result Category |
| Thomson, P. A.,2005(b) |
Single marker association:for SCZ, allele P-value = 0.31(all), P-value = 0.16(male), P-value = 0.0014(female) |
Association was not observed in SCZ, but was in observed SCZ(female). |
Negative |

Overlap with MDD from cross-disorder studies (count: 2)
| Reference |
Statistical Result |
Description |
Result Category |
| Macintyre, D. J.,2010 |
X2 goodness of fit test:P-value > 0.05 |
No significant association was observed. |
Negative
|
| Thomson, P. A.,2005(b) |
Single marker association:for MDD, allele P-value = 0.58(all), P-value = 0.19(male), P-value = 0.97(female) |
No association was observed. |
Negative
|