SNP Report

Basic Info

Name	rs4523957 dbSNP Ensembl
Location	chr17:2305605 - 2305605(1)
Variant Alleles	G/T
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.477037
Functional Annotation	intron_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000344595, ENST00000572709, ENST00000574987, ENST00000575840, ENST00000576620, ENST00000576848); upstream_gene_variant(ENST00000263073, ENST00000570662, ENST00000575692)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
SMG6	SMG6 nonsense mediated mRNA decay factor	17p13.3	Mapped by LD-proxy
HNRNPA1P16	heterogeneous nuclear ribonucleoprotein A1 pseudogene 16	17p13.3	Mapped by LD-proxy
SRR	serine racemase	17p13	1(0/1/0)

SNPs in LD with rs4523957 (count: 0) View in gBrowse (chr17:2305605..2305605 )

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

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