rs11682667

Homo sapiens
T>C
None
Check p-value
SNV (Single Nucleotide Variation)
C=0135 (4055/29984,GnomAD)
C=0126 (3671/29118,TOPMED)
C=0150 (749/5008,1000G)
C=0152 (586/3854,ALSPAC)
C=0156 (579/3708,TWINSUK)
chr2:129061896 (GRCh38.p7) (2q14.3)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 2NC_000002.12:g.129061896T>C
GRCh37.p13 chr 2NC_000002.11:g.129819469T>C

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 )
chr2129816620129816851E081-2618
chr2129816862129817043E081-2426
chr2129817169129817346E081-2123
chr2129817482129817532E081-1937
chr2129818688129818933E081-536
chr2129819138129819273E081-196
chr2129819325129820011E0810
chr2129820015129820096E081546
chr2129820167129820285E081698
chr2129820795129820907E0811326
chr2129820966129821048E0811497
chr2129825698129825803E0816229
chr2129844236129844415E08124767
chr2129844813129845306E08125344
chr2129819138129819273E082-196
chr2129819325129820011E0820
chr2129820015129820096E082546
chr2129820167129820285E082698
chr2129844813129845306E08225344


Mpgyi