SNP Report

Basic Info

Name	rs11665356 dbSNP Ensembl
Location	chr18:5886654 - 5886654(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.140375
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; upstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000581347); downstream_gene_variant(ENST00000383490); upstream_gene_variant(ENST00000577694, ENST00000580845, ENST00000582939)
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)
TMEM200C	transmembrane protein 200C	18p11.31	Mapped by Literature SNP

SNPs in LD with rs11665356 (count: 0) View in gBrowse (chr18:5886654..5886654 )

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

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