SNP Report

Basic Info

Name	rs11157046 dbSNP Ensembl
Location	chr14:39129763 - 39129763(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.096845
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000527381); intron_variant(ENST00000250379, ENST00000308317, ENST00000396249, ENST00000412033, ENST00000525153, ENST00000531684, ENST00000534684); NMD_transcript_variant(ENST00000412033, ENST00000525153, ENST00000531684); upstream_gene_variant(ENST00000524781, ENST00000524980, ENST00000529365)
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)
GEMIN2	gem (nuclear organelle) associated protein 2	14q21.1	1(0/1/0)

SNPs in LD with rs11157046 (count: 0) View in gBrowse (chr14:39129763..39129763 )

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

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