SNP Report

Basic Info
Name rs16952222 dbSNP Ensembl
Location chr18:7608053 - 7608053(1)
Variant Alleles C/T
Ancestral Allele T
Minor Allele T
Minor Allele Frequence 0.207069
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000332175, ENST00000580170)
No. of Studies 1 (Positive: 1; Negative: 0; 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
Mulle, J. G., 2007 allelic TDT X2=8.117, P-value = 0.0044 allelic TDT X2=8.117, P-value = 0.0044 No SNP in this analysis had an adjusted P-value < 0.05. Tran...... No SNP in this analysis had an adjusted P-value < 0.05. Transmission disequilibrium test analysis revealed no statistically significant association to SNPs or haplotypes within this region in this sample. More... Positive

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
PTPRM protein tyrosine phosphatase, receptor type, M 18p11.2 Mapped by Literature SNP

SNPs in LD with rs16952222 (count: 3) View in gBrowse (chr18:7597106..7608053 )
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: 3)

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

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