SNP Report

Basic Info

Name	rs4838811 dbSNP Ensembl
Location	chr22:50147013 - 50147013(1)
Variant Alleles	C/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.259185
Functional Annotation	5_prime_UTR_variant; downstream_gene_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript	5_prime_UTR_variant(ENST00000395852); downstream_gene_variant(ENST00000434497); intron_variant(ENST00000262794, ENST00000395858, ENST00000540615, ENST00000545383); upstream_gene_variant(ENST00000354853)
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)
MOV10L1	Mov10 RISC complex RNA helicase like 1	22q13.33	1(0/1/0)

SNPs in LD with rs4838811 (count: 0) View in gBrowse (chr22:50147013..50147013 )

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

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