SNP Report

Basic Info

Name	rs5522 dbSNP Ensembl
Location	chr4:148436323 - 148436323(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.108027
Functional Annotation	missense_variant; NMD_transcript_variant. Polyphen Annotation: benign(ENST00000342437, ENST00000344721, ENST00000358102, ENST00000511528, ENST00000512865, ENST00000625323) SIFT Annotation: tolerated - low confidence(ENST00000344721, ENST00000358102, ENST00000511528, ENST00000512865, ENST00000625323); tolerated(ENST00000342437)
Consequence to Transcript	missense_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 rs5522 (count: 0) View in gBrowse (chr4:148436323..148436323 )

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

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