SNP Report

Basic Info

Name	rs117255669 dbSNP Ensembl
Location	chr16:25227099 - 25227099(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.00499201
Functional Annotation	missense_variant. Polyphen Annotation: probably damaging(ENST00000219660, ENST00000566125) SIFT Annotation: deleterious(ENST00000219660, ENST00000566125)
Consequence to Transcript	missense_variant(ENST00000219660, ENST00000566125)
No. of Studies	1 (Positive: 0; Negative: 0; Trend: 1)
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
Georgi, B., 2014	G/A		7 in BPI, 1 in Well 7 in BPI, 1 in Well	Top 30 Amish-specific putative damaging exonic missense vari...... Top 30 Amish-specific putative damaging exonic missense variants by prevalence in affected individuals. More...	Trend

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
AQP8	aquaporin 8	16p12	1(0/0/1)

SNPs in LD with rs117255669 (count: 0) View in gBrowse (chr16:25227099..25227099 )

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

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