SNP Report

Basic Info

Name	rs11677858 dbSNP Ensembl
Location	chr2:154415941 - 154415941(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.111222
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000392825, ENST00000409237, ENST00000422126, ENST00000450838, ENST00000487047); non_coding_transcript_variant(ENST00000487047)
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)
GALNT13	polypeptide N-acetylgalactosaminyltransferase 13	2q24.1	1(0/1/0)

SNPs in LD with rs11677858 (count: 0) View in gBrowse (chr2:154415941..154415941 )

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

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