SNP Report

Basic Info

Name	rs17159262 dbSNP Ensembl
Location	chr7:30594717 - 30594717(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.0151757
Functional Annotation	5_prime_UTR_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	5_prime_UTR_variant(ENST00000389266, LRG_243t1); non_coding_transcript_exon_variant(ENST00000426529, ENST00000578994, ENST00000579174, ENST00000580440, ENST00000581665, ENST00000581794, ENST00000582549, ENST00000582733, ENST00000583664, ENST00000584199, ENST00000584372); non_coding_transcript_variant(ENST00000426529, ENST00000578994, ENST00000579174, ENST00000580440, ENST00000581665, ENST00000581794, ENST00000582549, ENST00000582733, ENST00000583664, ENST00000584199, ENST00000584372); upstream_gene_variant(ENST00000454308, ENST00000478124, ENST00000627489)
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)
GARS	glycyl-tRNA synthetase	7p15	Mapped by Literature SNP

SNPs in LD with rs17159262 (count: 0) View in gBrowse (chr7:30594717..30594717 )

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

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