SNP Detail Info-rs1782181

Organism: Homo sapiens

Alleles: G>A

Gene : Feature

None

p-value: Check p-value

Variation Type: SNV (Single Nucleotide Variation)

Frequency:

G==0248 (7432/29896,GnomAD)
G==0234 (6838/29118,TOPMED)
G==0257 (1289/5008,1000G)
G==0284 (1094/3854,ALSPAC)
G==0279 (1034/3708,TWINSUK)

Position: chr14:41227493 (GRCh38.p7) (14q21.1)

Phenotype: ND

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 14	NC_000014.9:g.41227493G>A
GRCh37.p13 chr 14	NC_000014.8:g.41696696G>A

Study	Population	Group	Sample #	Ref Allele	Alt Allele
1000Genomes	African	Sub	1322	G=0.182	A=0.818
1000Genomes	American	Sub	694	G=0.220	A=0.780
1000Genomes	East Asian	Sub	1008	G=0.303	A=0.697
1000Genomes	Europe	Sub	1006	G=0.263	A=0.737
1000Genomes	Global	Study-wide	5008	G=0.257	A=0.743
1000Genomes	South Asian	Sub	978	G=0.340	A=0.660
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.284	A=0.716
The Genome Aggregation Database	African	Sub	8722	G=0.210	A=0.790
The Genome Aggregation Database	American	Sub	838	G=0.180	A=0.820
The Genome Aggregation Database	East Asian	Sub	1608	G=0.300	A=0.700
The Genome Aggregation Database	Europe	Sub	18426	G=0.265	A=0.734
The Genome Aggregation Database	Global	Study-wide	29896	G=0.248	A=0.751
The Genome Aggregation Database	Other	Sub	302	G=0.240	A=0.760
Trans-Omics for Precision Medicine	Global	Study-wide	29118	G=0.234	A=0.765
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.279	A=0.721

rs1782181