SNP Report

Basic Info

Name	rs11608404 dbSNP Ensembl
Location	chr12:68690761 - 68690761(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.18111
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000481005, ENST00000540453); intron_variant(ENST00000229179, ENST00000378905, ENST00000535333, ENST00000535718, ENST00000537598, ENST00000538549, ENST00000539373, ENST00000539906, ENST00000545140); NMD_transcript_variant(ENST00000535718); non_coding_transcript_variant(ENST00000535333, ENST00000537598, ENST00000539373, ENST00000545140); upstream_gene_variant(ENST00000433116, ENST00000500695, ENST00000502102)
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)
NUP107	nucleoporin 107kDa	12q14	1(1/0/0)

SNPs in LD with rs11608404 (count: 0) View in gBrowse (chr12:68690761..68690761 )

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

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