SNP Report

Basic Info
Name rs2022268 dbSNP Ensembl
Location chr6:83563707 - 83563707(1)
Variant Alleles G/T
Ancestral Allele T
Minor Allele G
Minor Allele Frequence 0.183107
Functional Annotation intron_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000195649, ENST00000369694, ENST00000439399, ENST00000518312, ENST00000520213, ENST00000520302, ENST00000521485, ENST00000521616, ENST00000521743, ENST00000523448); NMD_transcript_variant(ENST00000518312, ENST00000521616)
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)
SNAP91 synaptosomal-associated protein, 91kDa 6q15 Mapped by LD-proxy

SNPs in LD with rs2022268 (count: 0) View in gBrowse (chr6:83563707..83563707 )

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

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