SNP Report

Basic Info

Name	rs1798977 dbSNP Ensembl
Location	chr13:50161840 - 50161840(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.422324
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000461527, ENST00000463474, ENST00000467721, ENST00000468168, ENST00000468522, ENST00000476738, ENST00000486895, ENST00000490577, ENST00000491341, ENST00000491615); non_coding_transcript_variant(ENST00000461527, ENST00000463474, ENST00000467721, ENST00000468168, ENST00000468522, ENST00000476738, ENST00000486895, ENST00000490577, ENST00000491341, ENST00000491615)
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)
DLEU1	deleted in lymphocytic leukemia 1 (non-protein coding)	13q14.3	Mapped by Literature SNP

SNPs in LD with rs1798977 (count: 0) View in gBrowse (chr13:50161840..50161840 )

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

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