BDgene

SNP Report

Basic Info
Name rs989713 dbSNP Ensembl
Location chr6:37681935 - 37681935(1)
Variant Alleles C/T
Ancestral Allele T
Minor Allele C
Minor Allele Frequence 0.113419
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000434837, ENST00000505425, ENST00000515437)
No. of Studies 1 (Positive: 0; Negative: 1; Trend: 0)
Source Literature
Overlap with SZ? YES
Overlap with MDD? YES

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result Category
Li, J.,2011(a) C/T Single SNP analyses: allele, P-value = 0.6927, OR[95%CI]=0.9...... Single SNP analyses: allele, P-value = 0.6927, OR[95%CI]=0.9633[0.8002, 1.1597], genotype, P-value = 0.2861 for BP More... 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)
MDGA1 MAM domain containing glycosylphosphatidylinositol anchor 1 6p21 1(1/0/0)

SNPs in LD with rs989713 (count: 5) View in gBrowse (chr6:37679868..37693265 )
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: 5)


Overlap with SZ from cross-disorder studies (count: 1)
Reference Statistical Result Description Result Category
Li, J.,2011(a) Single SNP analyses:allele, P-value = 0.2801, OR[95%CI]=1.1064[0.9209, 1.3294], genotype, P-value = 0.0969 for SZ No significant association was observed. Negative

Overlap with MDD from cross-disorder studies (count: 1)
Reference Statistical Result Description Result Category
Li, J.,2011(a) Single SNP analyses:allele, P-value = 0.0748, OR[95%CI]=1.1775[0.9837, 1.4094], genotype, P-value = 0.1617 for MDD No significant association was observed. Negative