SNP Report

Basic Info
Name rs7101690 dbSNP Ensembl
Location chr11:134124288 - 134124288(1)
Variant Alleles T/G
Ancestral Allele T
Minor Allele G
Minor Allele Frequence 0.154153
Functional Annotation intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000299106, ENST00000441717, ENST00000531302, ENST00000532252, ENST00000534549); NMD_transcript_variant(ENST00000532252); non_coding_transcript_exon_variant(ENST00000534330); non_coding_transcript_variant(ENST00000531302, ENST00000534330); upstream_gene_variant(ENST00000524969)
No. of Studies 0 (Positive: 0; Negative: 0; Trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
JAM3 junctional adhesion molecule 3 11q25 2(1/1/0)
PTP4A2P2 protein tyrosine phosphatase type IVA, member 2 pseudogene 2 11q24-q25 Mapped by LD-proxy

SNPs in LD with rs7101690 (count: 0) View in gBrowse (chr11:134124288..134124288 )

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

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