SNP Report

Basic Info

Name	rs934748 dbSNP Ensembl
Location	chr2:112600705 - 112600705(1)
Variant Alleles	G/A/C
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.419728
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000414784); non_coding_transcript_variant(ENST00000414784)
No. of Studies	1 (Positive: 0; Negative: 1; Trend: 0)
Source	Literature
Overlap with SZ?	NO
Overlap with MDD?	NO

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result Category
Gonzalez, S., 2014			Test for linkage:Â LOD=0.45,Â P-value=0.55;Â Test for associ...... Test for linkage:Â LOD=0.45,Â P-value=0.55;Â Test for association:Â LOD=1.56,Â P-value=0.007;Â Test for other linked variants:Â LOD=0.77,Â P-value=0.17 More...	No significant associations were observed. No significant associations were observed.	Negative

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
SLC20A1	solute carrier family 20 (phosphate transporter), member 1	2q13	1(0/1/0)
CHCHD5	coiled-coil-helix-coiled-coil-helix domain containing 5	2q14.1	1(0/1/0)

SNPs in LD with rs934748 (count: 0) View in gBrowse (chr2:112600705..112600705 )

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

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