SNP Report

Basic Info

Name	rs535586 dbSNP Ensembl
Location	chrCHR_HSCHR6_MHC_QBL_CTG1:31882939 - 31882939(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.166733
Functional Annotation	downstream_gene_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; splice_region_variant; synonymous_variant; intron_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000465429); non_coding_transcript_exon_variant(ENST00000463484, ENST00000480912); non_coding_transcript_variant(ENST00000463484, ENST00000480912); splice_region_variant(ENST00000375528, ENST00000375530, ENST00000375537, ENST00000395728, ENST00000463484, ENST00000480912); synonymous_variant(ENST00000375528, ENST00000375530, ENST00000375537, ENST00000395728, ENST00000476424, ENST00000466439, ENST00000498185, ENST00000466439, ENST00000498185, ENST00000415323, ENST00000421926, ENST00000440987, ENST00000450323, ENST00000466439, ENST00000498185, ENST00000415323, ENST00000421926, ENST00000440987, ENST00000450323, ENST00000495902, ENST00000495133, ENST00000497104, ENST00000495133, ENST00000497104, ENST00000420874, ENST00000436403, ENST00000443951, ENST00000450075, ENST00000495133, ENST00000497104, ENST00000420874, ENST00000436403, ENST00000443951, ENST00000450075, ENST00000480410, ENST00000484009, ENST00000497361, ENST00000484009, ENST00000497361, ENST00000420930, ENST00000428442, ENST00000429506, ENST00000450229, ENST00000484009, ENST00000497361, ENST00000420930, ENST00000428442, ENST00000429506, ENST00000450229, ENST00000475991, ENST00000462925, ENST00000467139, ENST00000462925, ENST00000467139, ENST00000420336, ENST00000427405, ENST00000446303, ENST00000454705, ENST00000462925, ENST00000467139, ENST00000420336, ENST00000427405, ENST00000446303, ENST00000454705, ENST00000494285); intron_variant(ENST00000489833, ENST00000469681, ENST00000497867, ENST00000469681, ENST00000489833, ENST00000497867, ENST00000383372, ENST00000383373, ENST00000400006, ENST00000400008, ENST00000469681, ENST00000497867, ENST00000383372, ENST00000383373, ENST00000400006, ENST00000400008)
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)
EHMT2	euchromatic histone-lysine N-methyltransferase 2	6p21.3	Mapped by Literature SNP

SNPs in LD with rs535586 (count: 0) View in gBrowse (chrCHR_HSCHR6_MHC_QBL_CTG1:31882939..31882939 )

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

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