SNP Report

Basic Info

Name	rs13376871 dbSNP Ensembl
Location	chr10:35080128 - 35080128(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.341653
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000374748, ENST00000374749, ENST00000374751, ENST00000374754, ENST00000468804, ENST00000626172); NMD_transcript_variant(ENST00000374754); non_coding_transcript_variant(ENST00000468804); upstream_gene_variant(ENST00000584484)
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)
MIR3611	microRNA 3611	10	Mapped by LD-proxy
CUL2	cullin 2	10p11.2	Mapped by LD-proxy

SNPs in LD with rs13376871 (count: 0) View in gBrowse (chr10:35080128..35080128 )

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

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