SNP Report

Basic Info

Name	rs174528 dbSNP Ensembl
Location	chr11:61776027 - 61776027(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.433906
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000265460, ENST00000278836, ENST00000535042); non_coding_transcript_variant(ENST00000535042); upstream_gene_variant(ENST00000389602, ENST00000536352, ENST00000537318, ENST00000546247)
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)
TMEM258	transmembrane protein 258	11q12.2	Mapped by Literature SNP
MYRF	myelin regulatory factor	11q12-q13.1	Mapped by Literature SNP

SNPs in LD with rs174528 (count: 0) View in gBrowse (chr11:61776027..61776027 )

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

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