SNP Detail Info-rs9873722

Organism: Homo sapiens

Alleles: A>G

Gene : Feature

None

p-value: Check p-value

Variation Type: SNV (Single Nucleotide Variation)

Frequency:

G=0136 (4083/29920,GnomAD)
G=0174 (5069/29118,TOPMED)
G=0148 (742/5008,1000G)
G=0104 (400/3854,ALSPAC)
G=0106 (394/3708,TWINSUK)

Position: chr3:164845602 (GRCh38.p7) (3q26.1)

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 3	NC_000003.12:g.164845602A>G
GRCh37.p13 chr 3	NC_000003.11:g.164563390A>G

Study	Population	Group	Sample #	Ref Allele	Alt Allele
1000Genomes	African	Sub	1322	A=0.722	G=0.278
1000Genomes	American	Sub	694	A=0.920	G=0.080
1000Genomes	East Asian	Sub	1008	A=0.905	G=0.095
1000Genomes	Europe	Sub	1006	A=0.907	G=0.093
1000Genomes	Global	Study-wide	5008	A=0.852	G=0.148
1000Genomes	South Asian	Sub	978	A=0.870	G=0.130
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.896	G=0.104
The Genome Aggregation Database	African	Sub	8698	A=0.746	G=0.254
The Genome Aggregation Database	American	Sub	836	A=0.940	G=0.060
The Genome Aggregation Database	East Asian	Sub	1600	A=0.897	G=0.102
The Genome Aggregation Database	Europe	Sub	18484	A=0.911	G=0.088
The Genome Aggregation Database	Global	Study-wide	29920	A=0.863	G=0.136
The Genome Aggregation Database	Other	Sub	302	A=0.910	G=0.090
Trans-Omics for Precision Medicine	Global	Study-wide	29118	A=0.825	G=0.174
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.894	G=0.106

rs9873722