rs2822582

Homo sapiens
T>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0478 (14311/29910,GnomAD)
T==0446 (13001/29118,TOPMED)
T==0423 (2117/5008,1000G)
G=0372 (1435/3854,ALSPAC)
G=0379 (1405/3708,TWINSUK)
chr21:14337293 (GRCh38.p7) (21q11.2)
AD
GWASdb2
1   publication(s)
See rs on genome
7 Enhancers around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 21NC_000021.9:g.14337293T>G
GRCh37.p13 chr 21NC_000021.8:g.15709614T>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 )
chr211575326415753417E06943650
chr211575358415753659E06943970
chr211575326415753417E07143650
chr211575358415753659E07143970
chr211575326415753417E07243650
chr211575326415753417E07443650
chr211575358415753659E07443970




Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr211575451715756862E06744903
chr211575451715756862E06844903
chr211575451715756862E06944903
chr211575451715756862E07044903
chr211575451715756862E07144903
chr211575451715756862E07244903
chr211575451715756862E07344903
chr211575451715756862E07444903
chr211575451715756862E08144903
chr211575451715756862E08244903










Mpgyi