SNP Report

Basic Info

Name	rs10223883 dbSNP Ensembl
Location	chr6:155099557 - 155099557(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.289736
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000318981, ENST00000461783, ENST00000528535, ENST00000535231, ENST00000538270, ENST00000545347)
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)
TIAM2	T-cell lymphoma invasion and metastasis 2	6q25	1(1/0/0)

SNPs in LD with rs10223883 (count: 0) View in gBrowse (chr6:155099557..155099557 )

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

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