SNP Report

Basic Info

Name	rs11625697 dbSNP Ensembl
Location	chr14:103998463 - 103998463(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.264776
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000339063, ENST00000409874, ENST00000557332)
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)
TDRD9	tudor domain containing 9	14q32.33	3(1/1/1)

SNPs in LD with rs11625697 (count: 0) View in gBrowse (chr14:103998463..103998463 )

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

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