SNP Report

Basic Info

Name	rs6959647 dbSNP Ensembl
Location	chr7:148833626 - 148833626(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.202276
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 rs6959647 (count: 0) View in gBrowse (chr7:148833626..148833626 )

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

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