SNP Report

Basic Info

Name	rs4669769 dbSNP Ensembl
Location	chr2:11677686 - 11677686(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.486422
Functional Annotation	missense_variant; upstream_gene_variant. Polyphen Annotation: benign(ENST00000449576) SIFT Annotation: tolerated - low confidence(ENST00000449576)
Consequence to Transcript	missense_variant(ENST00000449576); upstream_gene_variant(ENST00000435175, ENST00000455754, ENST00000617634)
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)
LPIN1	lipin 1	2p25.1	1(0/0/1)

SNPs in LD with rs4669769 (count: 0) View in gBrowse (chr2:11677686..11677686 )

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

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