SNP Report

Basic Info

Name	rs3867465 dbSNP Ensembl
Location	chr11:111791385 - 111791385(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.302316
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000398006, ENST00000524671, ENST00000525910, ENST00000526272, ENST00000527212, ENST00000531154, ENST00000532425, ENST00000614444, ENST00000616540, ENST00000619129, ENST00000622211); NMD_transcript_variant(ENST00000524671, ENST00000525910, ENST00000619129); non_coding_transcript_variant(ENST00000526272, ENST00000527212)
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)
ALG9	ALG9, alpha-1,2-mannosyltransferase	11q23	1(0/1/0)

SNPs in LD with rs3867465 (count: 0) View in gBrowse (chr11:111791385..111791385 )

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

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