SNP Report

Basic Info

Name	rs878152 dbSNP Ensembl
Location	chr4:148413406 - 148413406(1)
Variant Alleles	A/C
Ancestral Allele	A
Minor Allele	C
Minor Allele Frequence	0.0609026
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000342437, ENST00000344721, ENST00000358102, ENST00000511528, ENST00000512865, ENST00000625323); NMD_transcript_variant(ENST00000342437)
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)
NR3C2	nuclear receptor subfamily 3, group C, member 2	4q31	1(1/0/0)

SNPs in LD with rs878152 (count: 0) View in gBrowse (chr4:148413406..148413406 )

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

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