SNP Report

Basic Info

Name	rs174536 dbSNP Ensembl
Location	chr11:61784455 - 61784455(1)
Variant Alleles	A/C
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.305911
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000257262, ENST00000535297, ENST00000536352, ENST00000537318, ENST00000537328, ENST00000541893, ENST00000543510, ENST00000545210, ENST00000546247); intron_variant(ENST00000265460, ENST00000278836, ENST00000389602, ENST00000535042); non_coding_transcript_exon_variant(ENST00000539361); non_coding_transcript_variant(ENST00000535042, ENST00000539361)
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 rs174536 (count: 0) View in gBrowse (chr11:61784455..61784455 )

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

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