SNP Report

Basic Info

Name	rs2299123 dbSNP Ensembl
Location	chr7:39449136 - 39449136(1)
Variant Alleles	T/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.371006
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000403058, ENST00000416452, ENST00000518318, ENST00000524147, ENST00000559001); NMD_transcript_variant(ENST00000416452)
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)
POU6F2	POU class 6 homeobox 2	7p14.1	1(1/0/0)

SNPs in LD with rs2299123 (count: 0) View in gBrowse (chr7:39449136..39449136 )

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

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