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)