SNP Report

Basic Info
Name rs75758327 dbSNP Ensembl
Location chr2:167259287 - 167259287(1)
Variant Alleles G/C
Ancestral Allele G
Minor Allele C
Minor Allele Frequence 0.0930511
Functional Annotation 3_prime_UTR_variant; missense_variant.
Polyphen Annotation: benign(ENST00000409043, ENST00000409605, ENST00000409728)
SIFT Annotation: tolerated(ENST00000409043, ENST00000409605, ENST00000409728)
Consequence to Transcript 3_prime_UTR_variant(ENST00000295237, ENST00000409195, ENST00000409273, ENST00000628543); missense_variant(ENST00000409043, ENST00000409605, ENST00000409728)
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
Strauss, K. A., 2014 G/C Bipolar 1 disorder: X2=1.3, FBAT P-value=0.484, E...... Bipolar 1 disorder: X2=1.3, FBAT P-value=0.484, EMMAX P-value=0.465; Bipolar spectrum disorder: X4=2.6, FBAT P-value=0.408, EMMAX P-value=0.113 More... No significant associations were observed. No significant associations were observed. Negative

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
XIRP2 xin actin-binding repeat containing 2 2q31.1 1(0/1/0)

SNPs in LD with rs75758327 (count: 0) View in gBrowse (chr2:167259287..167259287 )

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

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