rs17685936

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0217 (6489/29906,GnomAD)
G=0191 (5572/29118,TOPMED)
G=0217 (1088/5008,1000G)
G=0268 (1033/3854,ALSPAC)
G=0259 (959/3708,TWINSUK)
chr19:29155013 (GRCh38.p7) (19q12)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 19NC_000019.10:g.29155013A>G
GRCh37.p13 chr 19NC_000019.9:g.29645920A>G

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 )
chr192961059029610811E070-35109
chr192961106529611763E070-34157
chr192961211329612157E070-33763
chr192960225929602309E081-43611
chr192960258229602703E081-43217
chr192962223229622710E081-23210
chr192962277729622863E081-23057
chr192962304129623137E081-22783
chr192962329429623344E081-22576
chr192967646929676533E08130549
chr192967663129676693E08130711
chr192967774729677811E08131827
chr192967794329678176E08132023
chr192967824429678320E08132324
chr192967842529678623E08132505
chr192967868729678863E08132767
chr192967889429678972E08132974
chr192967928629680427E08133366
chr192968076729680807E08134847
chr192968723229687562E08141312
chr192967928629680427E08233366
chr192968149729681547E08235577



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