SNP Report

Basic Info

Name	rs4818714 dbSNP Ensembl
Location	chr21:44361412 - 44361412(1)
Variant Alleles	G/A/C
Ancestral Allele	C
Minor Allele	A
Minor Allele Frequence	3.99361E-4
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000300481, ENST00000300482, ENST00000397928, ENST00000397932, ENST00000431901)
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)
TRPM2	transient receptor potential cation channel, subfamily M, member 2	21q22.3	5(3/2/0)

SNPs in LD with rs4818714 (count: 0) View in gBrowse (chr21:44361412..44361412 )

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

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