SNP Report

Basic Info

Name	rs10749689 dbSNP Ensembl
Location	chr1:53256192 - 53256192(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.371805
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000460214, ENST00000481431); intron_variant(ENST00000306052, ENST00000347547, ENST00000354412, ENST00000371454, ENST00000459674, ENST00000465675, ENST00000480045, ENST00000529670); NMD_transcript_variant(ENST00000480045, ENST00000529670); non_coding_transcript_variant(ENST00000459674)
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)
LRP8	low density lipoprotein receptor-related protein 8, apolipoprotein e receptor	1p32.3	1(1/0/0)

SNPs in LD with rs10749689 (count: 0) View in gBrowse (chr1:53256192..53256192 )

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

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