SNP Report

Basic Info

Name	rs487467 dbSNP Ensembl
Location	chr6:108228848 - 108228848(1)
Variant Alleles	A/C
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.215372
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000230085, ENST00000349379, ENST00000368979, ENST00000426155); NMD_transcript_variant(ENST00000368979)
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)
SNX3	sorting nexin 3	6q21	Mapped by Literature SNP

SNPs in LD with rs487467 (count: 0) View in gBrowse (chr6:108228848..108228848 )

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

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