SNP Report

Basic Info

Name	rs10949464 dbSNP Ensembl
Location	chr6:17841420 - 17841420(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.45647
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000259711, ENST00000378814, ENST00000378826, ENST00000378843, ENST00000636847)
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)
KIF13A	kinesin family member 13A	6p23	2(0/1/1)

SNPs in LD with rs10949464 (count: 0) View in gBrowse (chr6:17841420..17841420 )

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

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