SNP Report

Basic Info

Name	rs2442735 dbSNP Ensembl
Location	chrCHR_HSCHR6_MHC_SSTO_CTG1:31372564 - 31372564(1)
Variant Alleles	A/G
Minor Allele	G
Minor Allele Frequence	0.0397364
Functional Annotation	downstream_gene_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000425174, ENST00000449999); upstream_gene_variant(ENST00000424108, ENST00000417754, ENST00000434840, ENST00000449890, ENST00000430251, ENST00000440712, ENST00000433773, ENST00000419729, ENST00000454711, ENST00000423129, ENST00000416556, ENST00000447153, ENST00000427014)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ZDHHC20P2	zinc finger, DHHC-type containing 20 pseudogene 2	6p21.3	Mapped by Literature SNP
FGFR3P1	fibroblast growth factor receptor 3 pseudogene 1	6p21.33	Mapped by LD-proxy
HLA-S	major histocompatibility complex, class I, S (pseudogene)	6p21.3	Mapped by Literature SNP

SNPs in LD with rs2442735 (count: 0) View in gBrowse (chrCHR_HSCHR6_MHC_SSTO_CTG1:31372564..31372564 )

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

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