SNP Report

Basic Info

Name	rs4398822 dbSNP Ensembl
Location	chr7:102926722 - 102926722(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.0551118
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000249377, ENST00000313221, ENST00000339431, ENST00000379305, ENST00000379308, ENST00000436908, ENST00000448002, ENST00000455112, ENST00000456695, ENST00000468216, ENST00000477915, ENST00000498487); NMD_transcript_variant(ENST00000448002); non_coding_transcript_variant(ENST00000468216, ENST00000477915, ENST00000498487)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
LRRC17	leucine rich repeat containing 17	7q22.1	Mapped by LD-proxy
FBXL13	F-box and leucine-rich repeat protein 13	7q22.1	Mapped by LD-proxy

SNPs in LD with rs4398822 (count: 0) View in gBrowse (chr7:102926722..102926722 )

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

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