SNP Report

Basic Info

Name	rs1926032 dbSNP Ensembl
Location	chr10:103069712 - 103069712(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.13758
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000369878, ENST00000433628, ENST00000475511); non_coding_transcript_variant(ENST00000475511)
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 rs1926032 (count: 0) View in gBrowse (chr10:103069712..103069712 )

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

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