SNP Report

Basic Info

Name	rs6518192 dbSNP Ensembl
Location	chr21:44471334 - 44471334(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.24381
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000445440); intron_variant(ENST00000443300); non_coding_transcript_variant(ENST00000443300); upstream_gene_variant(ENST00000443620)
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)
MTND5P1	MT-ND5 pseudogene 1	21q22.3	Mapped by LD-proxy
MTND6P21	MT-ND6 pseudogene 21	21q22.3	Mapped by LD-proxy

SNPs in LD with rs6518192 (count: 0) View in gBrowse (chr21:44471334..44471334 )

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

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