SNP Report

Basic Info

Name	rs2444898 dbSNP Ensembl
Location	chr8:98015449 - 98015449(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.126997
Functional Annotation	intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000254898, ENST00000518154, ENST00000520016, ENST00000521689, ENST00000521952, ENST00000522025, ENST00000524308); NMD_transcript_variant(ENST00000521952); upstream_gene_variant(ENST00000517321)
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)
MATN2	matrilin 2	8q22.1-q22.2	Mapped by Literature SNP

SNPs in LD with rs2444898 (count: 0) View in gBrowse (chr8:98015449..98015449 )

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

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