BDgene

SNP Report

Basic Info
Name rs6908950 dbSNP Ensembl
Location chr6:42758611 - 42758611(1)
Variant Alleles G/C
Ancestral Allele T
Minor Allele C
Minor Allele Frequence 0.352636
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000614467)
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)
GLTSCR1L GLTSCR1-like 6p21.1 Mapped by Literature SNP

SNPs in LD with rs6908950 (count: 0) View in gBrowse (chr6:42758611..42758611 )

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

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