rs11691730

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0209 (6274/29890,GnomAD)
A=0254 (7403/29116,TOPMED)
A=0270 (1354/5008,1000G)
A=0143 (550/3854,ALSPAC)
A=0128 (474/3708,TWINSUK)
chr2:102944668 (GRCh38.p7) (2q12.1)
ND
GWASdb2
1   publication(s)
See rs on genome
1 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 2NC_000002.12:g.102944668G>A
GRCh37.p13 chr 2NC_000002.11:g.103561126G>A

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr2103592344103593549E06831218
chr2103593710103594123E06832584
chr2103596138103596188E06935012
chr2103592344103593549E07031218
chr2103593710103594123E07032584
chr2103595206103595439E07134080
chr2103596138103596188E07135012
chr2103596138103596188E07235012
chr2103596138103596188E07435012
chr2103548964103549294E081-11832
chr2103590416103590470E08129290
chr2103590754103590992E08129628
chr2103592344103593549E08131218
chr2103594485103594929E08133359
chr2103596138103596188E08135012
chr2103590416103590470E08229290
chr2103590754103590992E08229628
chr2103592344103593549E08231218
chr2103593710103594123E08232584
chr2103609782103609863E08248656








Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr2103594177103594428E08133051

Mpgyi