SNP Report

Basic Info

Name	rs4385986 dbSNP Ensembl
Location	chr12:106739997 - 106739997(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.35024
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000229387, ENST00000357881, ENST00000392842, ENST00000549203, ENST00000551505); non_coding_transcript_variant(ENST00000549203, ENST00000551505)
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)
RFX4	regulatory factor X, 4 (influences HLA class II expression)	12q24	2(1/1/0)

SNPs in LD with rs4385986 (count: 0) View in gBrowse (chr12:106739997..106739997 )

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

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