SNP Report

Basic Info

Name	rs10158822 dbSNP Ensembl
Location	chr1:236886876 - 236886876(1)
Variant Alleles	T/G
Ancestral Allele	T
Minor Allele	G
Minor Allele Frequence	0.218251
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000366576, ENST00000366577, ENST00000535889)
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)
MTR	5-methyltetrahydrofolate-homocysteine methyltransferase	1q43	2(1/1/0)

SNPs in LD with rs10158822 (count: 0) View in gBrowse (chr1:236886876..236886876 )

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

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