SNP Report

Basic Info

Name	rs2061052 dbSNP Ensembl
Location	chr8:98040797 - 98040797(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.126597
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000254898, ENST00000287038, ENST00000384339, ENST00000396070, ENST00000517489, ENST00000517805, ENST00000518154, ENST00000518850, ENST00000520016, ENST00000520998, ENST00000521112, ENST00000521291, ENST00000521534, ENST00000521689, ENST00000521726, ENST00000522025, ENST00000522156, ENST00000523172, ENST00000523561, ENST00000524308); intron_variant(ENST00000518164); non_coding_transcript_variant(ENST00000518164); upstream_gene_variant(ENST00000501016)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
RPL30	ribosomal protein L30	8q22	Mapped by Literature SNP
SNORA72	small nucleolar RNA, H/ACA box 72	8q22.2	Mapped by LD-proxy
MATN2	matrilin 2	8q22.1-q22.2	Mapped by Literature SNP

SNPs in LD with rs2061052 (count: 0) View in gBrowse (chr8:98040797..98040797 )

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

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