SNP Report

Basic Info
Name rs17647803 dbSNP Ensembl
Location chr10:81980465 - 81980465(1)
Variant Alleles A/G
Ancestral Allele A
Minor Allele G
Minor Allele Frequence 0.0461262
Functional Annotation intron_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000372141, ENST00000372142, ENST00000404547, ENST00000404576, ENST00000555784, ENST00000556918, ENST00000602794); NMD_transcript_variant(ENST00000555784, ENST00000602794)
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
Xu, W., 2014 G/A P-value=5.53E-06 P-value=5.53E-06 Top 132 SNPs (showing suggestive association to BD in our CA...... Top 132 SNPs (showing suggestive association to BD in our CAMH family cohort: p<0.0001). More... Negative

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
NRG3 neuregulin 3 10q23.1 2(0/2/0)

SNPs in LD with rs17647803 (count: 16) View in gBrowse (chr10:81930279..81994996 )
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: 16)

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

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