SNP Report

Basic Info

Name	rs1873091 dbSNP Ensembl
Location	chr4:55605266 - 55605266(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.145168
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000264218, ENST00000505262, ENST00000507338, ENST00000509371, ENST00000511469, ENST00000515325); non_coding_transcript_variant(ENST00000509371, ENST00000515325)
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)
NMU	neuromedin U	4q12	Mapped by LD-proxy

SNPs in LD with rs1873091 (count: 0) View in gBrowse (chr4:55605266..55605266 )

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

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