SNP Report

Basic Info

Name	rs7311054 dbSNP Ensembl
Location	chr12:126738496 - 126738496(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.165535
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000535118, ENST00000537374, ENST00000539315, ENST00000540684, ENST00000541359); non_coding_transcript_variant(ENST00000535118, ENST00000537374, ENST00000539315, ENST00000540684, ENST00000541359); upstream_gene_variant(ENST00000345111, ENST00000535544, ENST00000540250, ENST00000544499, ENST00000546117)
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)
LINC00943	long intergenic non-protein coding RNA 943	12q24.32	Mapped by Literature SNP
LINC00944	long intergenic non-protein coding RNA 944	12q24.32	Mapped by Literature SNP

SNPs in LD with rs7311054 (count: 0) View in gBrowse (chr12:126738496..126738496 )

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

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