SNP Report

Basic Info

Name	rs11683093 dbSNP Ensembl
Location	chr2:2199453 - 2199453(1)
Variant Alleles	A/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.151957
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000399161, ENST00000428368, ENST00000479156); non_coding_transcript_variant(ENST00000479156)
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)
MYT1L	myelin transcription factor 1-like	2p25.3	1(1/0/0)

SNPs in LD with rs11683093 (count: 0) View in gBrowse (chr2:2199453..2199453 )

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

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