SNP Report

Basic Info

Name	rs138155176 dbSNP Ensembl
Location	chr7:121271384 - 121271384(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	7.98722E-4
Functional Annotation	missense_variant. Polyphen Annotation: probably damaging(ENST00000310396) SIFT Annotation: deleterious(ENST00000310396)
Consequence to Transcript	missense_variant(ENST00000310396)
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, 6 in Well, GERP=5.93 7 in BPI, 6 in Well, GERP=5.93	Top 30 Amish-specific putative damaging exonic missense vari...... Top 30 Amish-specific putative damaging exonic missense variants by prevalence in affected individuals. Putative damaging exonic variants found in the five linkage regions. More...	Trend

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
CPED1	cadherin-like and PC-esterase domain containing 1	7q31.31	1(0/0/1)

SNPs in LD with rs138155176 (count: 0) View in gBrowse (chr7:121271384..121271384 )

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

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