SNP Report

Basic Info

Name	rs11191593 dbSNP Ensembl
Location	chr10:103179458 - 103179458(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.156949
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000412473); intron_variant(ENST00000343289, ENST00000369857, ENST00000452156, ENST00000461461, ENST00000467380, ENST00000470299); NMD_transcript_variant(ENST00000452156, ENST00000461461); non_coding_transcript_variant(ENST00000369857, ENST00000467380); upstream_gene_variant(ENST00000404739)
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)
MARCKSL1P1	MARCKS-like 1 pseudogene 1	10q24.33	Mapped by LD-proxy
NT5C2	5'-nucleotidase, cytosolic II	10q24.32	2(2/0/0)

SNPs in LD with rs11191593 (count: 0) View in gBrowse (chr10:103179458..103179458 )

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

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