BDgene

SNP Report

Basic Info
Name rs11111272 dbSNP Ensembl
Location chr12:102433663 - 102433663(1)
Variant Alleles G/C
Ancestral Allele G
Minor Allele G
Minor Allele Frequence 0.364018
Functional Annotation intron_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000307046, ENST00000337514, ENST00000392904, ENST00000392905, ENST00000424202, ENST00000456098, ENST00000635615); non_coding_transcript_variant(ENST00000635615)
No. of Studies 1 (Positive: 0; Negative: 1; Trend: 0)
Source Literature
Overlap with SZ? NO
Overlap with MDD? NO

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result Category
Pereira, A. C.,2011 G/C X2 tests: X2=0.014, P-value = 0.907 X2 tests: X2=0.014, P-value = 0.907 No significant association was observed. No significant association was observed. Negative

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
IGF1 insulin-like growth factor 1 (somatomedin C) 12q23.2 1(1/0/0)

SNPs in LD with rs11111272 (count: 11) View in gBrowse (chr12:102405458..102456445 )
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.

Literature-origin SNPs (count: 0)

LD-proxies (count: 11)


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

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

Copyright: Bioinformatics Lab, Institute of Psychology, Chinese Academy of Sciences Feedback Acknowledgements
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Last update: March 31, 2016