BDgene

SNP Report

Basic Info
Name rs17110747 dbSNP Ensembl
Location chr12:72032174 - 72032174(1)
Variant Alleles G/A
Ancestral Allele G
Minor Allele A
Minor Allele Frequence 0.145367
Functional Annotation 3_prime_UTR_variant; intron_variant; non_coding_transcript_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000333850); intron_variant(ENST00000547278, ENST00000547348, ENST00000550403, ENST00000551074); non_coding_transcript_variant(ENST00000547278, ENST00000547348, ENST00000550403, ENST00000551074)
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
Lin, Y. M., 2007 G/A chi-square P-value = 0.07 chi-square P-value = 0.07 this SNP was not associated with the disease this SNP was not associated with the disease Negative

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
TPH2 tryptophan hydroxylase 2 12q15 13(10/3/0)

SNPs in LD with rs17110747 (count: 5) View in gBrowse (chr12:72032174..72109907 )
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: 0)

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