SNP Report

Basic Info

Name	rs2391870 dbSNP Ensembl
Location	chr7:30501416 - 30501416(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.378594
Functional Annotation	intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000005374, ENST00000275428, ENST00000409144, ENST00000409390, ENST00000409436, ENST00000440082, ENST00000447901, ENST00000598361); NMD_transcript_variant(ENST00000440082, ENST00000447901); upstream_gene_variant(ENST00000426081)
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)
GGCT	gamma-glutamylcyclotransferase	7p15-p14	Mapped by LD-proxy

SNPs in LD with rs2391870 (count: 0) View in gBrowse (chr7:30501416..30501416 )

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

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