SNP Report

Basic Info

Name	rs3746435 dbSNP Ensembl
Location	chr20:34999395 - 34999395(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.171526
Functional Annotation	downstream_gene_variant; missense_variant; upstream_gene_variant. Polyphen Annotation: probably damaging(ENST00000262873, ENST00000618182) SIFT Annotation: deleterious(ENST00000262873, ENST00000618182)
Consequence to Transcript	downstream_gene_variant(ENST00000252015, ENST00000451813); missense_variant(ENST00000262873, ENST00000618182); upstream_gene_variant(ENST00000433934, ENST00000435272, ENST00000446156, ENST00000453028, ENST00000456649)
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)
TRPC4AP	transient receptor potential cation channel, subfamily C, member 4 associated protein	20q11.23	1(1/0/0)
MYH7B	myosin, heavy chain 7B, cardiac muscle, beta	20q11	Mapped by LD-proxy

SNPs in LD with rs3746435 (count: 0) View in gBrowse (chr20:34999395..34999395 )

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

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