SNP Report

Basic Info
Name rs1150789 dbSNP Ensembl
Location chr6:37212579 - 37212579(1)
Variant Alleles G/A
Ancestral Allele G
Minor Allele G
Minor Allele Frequence 0.448482
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000336655, ENST00000356757); downstream_gene_variant(ENST00000478262); non_coding_transcript_exon_variant(ENST00000497775); non_coding_transcript_variant(ENST00000497775)
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)
TMEM217 transmembrane protein 217 6p21.31-p21.2 1(0/0/1)

SNPs in LD with rs1150789 (count: 0) View in gBrowse (chr6:37212579..37212579 )

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

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