SNP Report

Basic Info

Name	rs929493 dbSNP Ensembl
Location	chr10:117259615 - 117259615(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.416933
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000298472, ENST00000497497); non_coding_transcript_variant(ENST00000497497)
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)
SLC18A2	solute carrier family 18 (vesicular monoamine transporter), member 2	10q25	1(1/0/0)

SNPs in LD with rs929493 (count: 0) View in gBrowse (chr10:117259615..117259615 )

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

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