SNP Report

Basic Info

Name	rs1060330 dbSNP Ensembl
Location	chr3:52254929 - 52254929(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.492412
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000296490); downstream_gene_variant(ENST00000296487, ENST00000323588, ENST00000409502, ENST00000467471, ENST00000469000, ENST00000482724, ENST00000487402, ENST00000489606)
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)
PPM1M	protein phosphatase, Mg2+/Mn2+ dependent, 1M	3p21.31	Mapped by Literature SNP
WDR82	WD repeat domain 82	3p21.2	Mapped by Literature SNP

SNPs in LD with rs1060330 (count: 0) View in gBrowse (chr3:52254929..52254929 )

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

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