SNP Report

Basic Info

Name	rs10437344 dbSNP Ensembl
Location	chr10:62352931 - 62352931(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.291733
Functional Annotation	downstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000496150)
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)
RN7SL591P	RNA, 7SL, cytoplasmic 591, pseudogene	10q21.2	Mapped by LD-proxy

SNPs in LD with rs10437344 (count: 0) View in gBrowse (chr10:62352931..62352931 )

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

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