SNP Report

Basic Info

Name	rs16996127 dbSNP Ensembl
Location	chr19:19516501 - 19516501(1)
Variant Alleles	T/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.204273
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000428459, ENST00000502506, ENST00000503283, ENST00000507754, ENST00000511180, ENST00000511584, ENST00000555938, ENST00000586674, ENST00000606722); NMD_transcript_variant(ENST00000502506, ENST00000606722); non_coding_transcript_variant(ENST00000511180, ENST00000511584, ENST00000586674); upstream_gene_variant(ENST00000585580, ENST00000587522, ENST00000602623)
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)
NDUFA13	NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13	19p13.11	Mapped by LD-proxy
TSSK6	testis-specific serine kinase 6	19p13.11	Mapped by LD-proxy

SNPs in LD with rs16996127 (count: 0) View in gBrowse (chr19:19516501..19516501 )

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

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