SNP Report

Basic Info

Name	rs10215794 dbSNP Ensembl
Location	chr7:148781803 - 148781803(1)
Variant Alleles	C/G
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.271765
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000325222, ENST00000409469, ENST00000602748, ENST00000617797)
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)
CUL1	cullin 1	7q36.1	1(1/0/0)

SNPs in LD with rs10215794 (count: 0) View in gBrowse (chr7:148781803..148781803 )

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

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