SNP Report

Basic Info

Name	rs7165988 dbSNP Ensembl
Location	chr15:38696614 - 38696614(1)
Variant Alleles	C/G/T
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.194089
Functional Annotation	missense_variant; synonymous_variant. Polyphen Annotation: possibly damaging(ENST00000318792) SIFT Annotation: tolerated - low confidence(ENST00000318792)
Consequence to Transcript	missense_variant(ENST00000318792); synonymous_variant(ENST00000318792)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
C15orf53	chromosome 15 open reading frame 53	15q14	3(0/1/2)

SNPs in LD with rs7165988 (count: 0) View in gBrowse (chr15:38696614..38696614 )

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

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