SNP Report

Basic Info
Name rs4726996 dbSNP Ensembl
Location chr7:148868571 - 148868571(1)
Variant Alleles G/A
Ancestral Allele A
Minor Allele G
Minor Allele Frequence 0.198882
Functional Annotation intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000320356, ENST00000350995, ENST00000460911, ENST00000476773, ENST00000478654, ENST00000483012, ENST00000483967, ENST00000492143, ENST00000498186, LRG_531t1); NMD_transcript_variant(ENST00000483012, ENST00000492143); non_coding_transcript_variant(ENST00000498186)
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)
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit 7q35-q36 Mapped by LD-proxy

SNPs in LD with rs4726996 (count: 0) View in gBrowse (chr7:148868571..148868571 )

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

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