SNP Report

Basic Info

Name	rs84473 dbSNP Ensembl
Location	chr22:38161319 - 38161319(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.456669
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000332509, ENST00000335539, ENST00000402064, ENST00000417303, ENST00000420435, ENST00000426674, ENST00000430886, ENST00000435484, ENST00000436218, ENST00000445591, ENST00000447598, ENST00000452972, ENST00000455341, ENST00000471636, ENST00000479641); non_coding_transcript_variant(ENST00000420435, ENST00000426674, ENST00000445591, ENST00000452972, ENST00000471636, ENST00000479641)
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)
PLA2G6	phospholipase A2, group VI (cytosolic, calcium-independent)	22q13.1	2(1/1/0)

SNPs in LD with rs84473 (count: 0) View in gBrowse (chr22:38161319..38161319 )

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

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