SNP Report

Basic Info

Name	rs9821675 dbSNP Ensembl
Location	chr3:49865111 - 49865111(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.404752
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000296471, ENST00000463537, ENST00000466535, ENST00000466940, ENST00000467248, ENST00000475665, ENST00000476105, ENST00000477224, ENST00000479704, ENST00000480398, ENST00000487726, ENST00000488336, ENST00000498324); NMD_transcript_variant(ENST00000466535, ENST00000487726); non_coding_transcript_variant(ENST00000475665, ENST00000476105, ENST00000479704, ENST00000498324); upstream_gene_variant(ENST00000472895, ENST00000478149, ENST00000483811, ENST00000584520, ENST00000620470)
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)
CAMKV	CaM kinase-like vesicle-associated	3p21.31	Mapped by Literature SNP
RN7SL217P	RNA, 7SL, cytoplasmic 217, pseudogene	3p21.31	Mapped by LD-proxy

SNPs in LD with rs9821675 (count: 0) View in gBrowse (chr3:49865111..49865111 )

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

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