SNP Report

Basic Info

Name	rs11214005 dbSNP Ensembl
Location	chr11:111800134 - 111800134(1)
Variant Alleles	A/C
Ancestral Allele	A
Minor Allele	C
Minor Allele Frequence	0.316693
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 rs11214005 (count: 0) View in gBrowse (chr11:111800134..111800134 )

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

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