SNP Report

Basic Info

Name	rs9458841 dbSNP Ensembl
Location	chr6:163513113 - 163513113(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.0373403
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000275262, ENST00000361195, ENST00000361752, ENST00000361758, ENST00000392127, ENST00000424802, ENST00000453779, ENST00000537041, ENST00000537883, ENST00000544436, ENST00000544823, ENST00000545346, ENST00000545607); NMD_transcript_variant(ENST00000361758, ENST00000545346, ENST00000545607)
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)
QKI	QKI, KH domain containing, RNA binding	6q26	1(0/1/0)

SNPs in LD with rs9458841 (count: 0) View in gBrowse (chr6:163513113..163513113 )

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

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