SNP Report

Basic Info

Name	rs17115213 dbSNP Ensembl
Location	chr10:102921386 - 102921386(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.152157
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000369875, ENST00000369878, ENST00000433628)
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)
CNNM2	cyclin and CBS domain divalent metal cation transport mediator 2	10q24.32	Mapped by Literature SNP

SNPs in LD with rs17115213 (count: 0) View in gBrowse (chr10:102921386..102921386 )

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

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