SNP Report

Basic Info

Name	rs4798791 dbSNP Ensembl
Location	chr18:9255984 - 9255984(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.386581
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; missense_variant; NMD_transcript_variant; upstream_gene_variant. Polyphen Annotation: probably damaging(ENST00000262126, ENST00000400020) SIFT Annotation: tolerated - low confidence(ENST00000262126, ENST00000400020)
Consequence to Transcript	3_prime_UTR_variant(ENST00000359158); downstream_gene_variant(ENST00000546007, ENST00000578850); missense_variant(ENST00000262126, ENST00000400020); NMD_transcript_variant(ENST00000359158); upstream_gene_variant(ENST00000609701)
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)
ANKRD12	ankyrin repeat domain 12	18p11.22	Mapped by Literature SNP

SNPs in LD with rs4798791 (count: 0) View in gBrowse (chr18:9255984..9255984 )

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

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