SNP Report

Basic Info

Name	rs10893378 dbSNP Ensembl
Location	chr11:125426505 - 125426505(1)
Variant Alleles	C/G
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.342053
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000298282, ENST00000526955, ENST00000530517, ENST00000531116, ENST00000532623); NMD_transcript_variant(ENST00000532623); non_coding_transcript_variant(ENST00000526955, ENST00000530517, ENST00000531116)
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)
PKNOX2	PBX/knotted 1 homeobox 2	11q24.2	Mapped by LD-proxy

SNPs in LD with rs10893378 (count: 0) View in gBrowse (chr11:125426505..125426505 )

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

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