SNP Report

Basic Info

Name	rs11933380 dbSNP Ensembl
Location	chr4:148076251 - 148076251(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.401358
Functional Annotation	downstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000336498, ENST00000342437, ENST00000344721, ENST00000358102, ENST00000506020, ENST00000506054, ENST00000507661, ENST00000510076, ENST00000512865, ENST00000625323)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ARHGAP10	Rho GTPase activating protein 10	4q31.23	Mapped by Literature SNP
NR3C2	nuclear receptor subfamily 3, group C, member 2	4q31	1(1/0/0)

SNPs in LD with rs11933380 (count: 0) View in gBrowse (chr4:148076251..148076251 )

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

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