SNP Report

Basic Info

Name	rs2451361 dbSNP Ensembl
Location	chr6:34061427 - 34061427(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.334465
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000374177, ENST00000374181, ENST00000455714, ENST00000535756, ENST00000538487, ENST00000544773, ENST00000545715, ENST00000609222, ENST00000609278, ENST00000609443, ENST00000609860); NMD_transcript_variant(ENST00000609278); non_coding_transcript_exon_variant(ENST00000609973); non_coding_transcript_variant(ENST00000545715, ENST00000609860, ENST00000609973)
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)
GRM4	glutamate receptor, metabotropic 4	6p21.3	2(2/0/0)

SNPs in LD with rs2451361 (count: 0) View in gBrowse (chr6:34061427..34061427 )

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

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