SNP Report

Basic Info

Name	rs11919197 dbSNP Ensembl
Location	chr3:51702328 - 51702328(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.0856629
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000444233, ENST00000457927); intron_variant(ENST00000341333, ENST00000395057, ENST00000415259, ENST00000416589, ENST00000457573, ENST00000463857, ENST00000489026, ENST00000493444, ENST00000611400, ENST00000614067); non_coding_transcript_variant(ENST00000463857, ENST00000489026, ENST00000493444); upstream_gene_variant(ENST00000296479, ENST00000395052, ENST00000464585, ENST00000475478)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
GRM2	glutamate receptor, metabotropic 2	3p21.2	1(0/1/0)
TEX264	testis expressed 264	3p21	Mapped by Literature SNP

SNPs in LD with rs11919197 (count: 0) View in gBrowse (chr3:51702328..51702328 )

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

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