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)