SNP Report

Basic Info

Name	rs6026565 dbSNP Ensembl
Location	chr20:58864253 - 58864253(1)
Variant Alleles	T/A
Ancestral Allele	T
Minor Allele	A
Minor Allele Frequence	0.096246
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000313949, ENST00000349036, ENST00000371075, ENST00000371098, ENST00000371100, ENST00000371102, ENST00000419558, ENST00000423897, ENST00000441270, ENST00000450130, ENST00000453292, ENST00000462499, ENST00000464624, ENST00000467227, ENST00000472183, ENST00000481768, ENST00000482112, ENST00000490374, ENST00000491348, ENST00000493744); non_coding_transcript_variant(ENST00000441270, ENST00000462499, ENST00000464624, ENST00000467227, ENST00000472183, ENST00000481768, ENST00000482112, ENST00000490374, ENST00000491348, ENST00000493744)
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
McDonald, M. L.,2012			chi square test:OR(95%CI) = 1.3(1.1â€“1.5),P-value = 0.0017 ...... chi square test:OR(95%CI) = 1.3(1.1â€“1.5),P-value = 0.0017 for BD-I 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)
GNAS	GNAS complex locus	20q13.2-q13.3	1(0/1/0)

SNPs in LD with rs6026565 (count: 0) View in gBrowse (chr20:58864253..58864253 )

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

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