SNP Detail Info-rs9584182

Organism: Homo sapiens

Alleles: A>G

Gene : Feature

LOC105370301 : Intron Variant

p-value: Check p-value

Variation Type: SNV (Single Nucleotide Variation)

Frequency:

G=0132 (3955/29896,GnomAD)
G=0164 (4800/29118,TOPMED)
G=0133 (668/5008,1000G)
G=0105 (403/3854,ALSPAC)
G=0102 (379/3708,TWINSUK)

Position: chr13:87040002 (GRCh38.p7) (13q31.1)

Phenotype: AD

Dataset:

GWASdb2

Publications: 1 publication(s)

Genomic View: See rs on genome

Enhancer: 0 Enhancer around

Promoter: 0 Promoter around

Sequence Name	Change(s)
GRCh38.p7 chr 13	NC_000013.11:g.87040002A>G
GRCh37.p13 chr 13	NC_000013.10:g.87692257A>G

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105370301 transcript variant X1	XR_931623.2:n.	N/A	Intron Variant
LOC105370301 transcript variant X2	XR_931624.1:n.	N/A	Intron Variant

Study	Population	Group	Sample #	Ref Allele	Alt Allele
1000Genomes	African	Sub	1322	A=0.710	G=0.290
1000Genomes	American	Sub	694	A=0.910	G=0.090
1000Genomes	East Asian	Sub	1008	A=0.969	G=0.031
1000Genomes	Europe	Sub	1006	A=0.906	G=0.094
1000Genomes	Global	Study-wide	5008	A=0.867	G=0.133
1000Genomes	South Asian	Sub	978	A=0.900	G=0.100
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.895	G=0.105
The Genome Aggregation Database	African	Sub	8678	A=0.748	G=0.252
The Genome Aggregation Database	American	Sub	836	A=0.930	G=0.070
The Genome Aggregation Database	East Asian	Sub	1618	A=0.954	G=0.046
The Genome Aggregation Database	Europe	Sub	18464	A=0.913	G=0.086
The Genome Aggregation Database	Global	Study-wide	29896	A=0.867	G=0.132
The Genome Aggregation Database	Other	Sub	300	A=0.850	G=0.150
Trans-Omics for Precision Medicine	Global	Study-wide	29118	A=0.835	G=0.164
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.898	G=0.102

rs9584182