SNP Report

Basic Info
Name rs420436 dbSNP Ensembl
Location chrCHR_HSCHR6_MHC_COX_CTG1:28588216 - 28588216(1)
Variant Alleles A/G
Ancestral Allele G
Minor Allele G
Minor Allele Frequence 0.0694888
Functional Annotation intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000499525, ENST00000524745, ENST00000530247); non_coding_transcript_variant(ENST00000499525, ENST00000524745, ENST00000530247); upstream_gene_variant(ENST00000452236, ENST00000526291, ENST00000619431, ENST00000619431, ENST00000508341)
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)
SCAND3 zinc finger, BED-type containing 9 6p21.33 Mapped by LD-proxy

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

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