rs2733022

Homo sapiens
T>C
None
Check p-value
SNV (Single Nucleotide Variation)
C=0100 (3007/29898,GnomAD)
C=0115 (3376/29118,TOPMED)
C=0069 (346/5008,1000G)
C=0088 (341/3854,ALSPAC)
C=0094 (347/3708,TWINSUK)
chr8:5724652 (GRCh38.p7) (8p23.2)
AD
GWASdb2
1   publication(s)
See rs on genome
8 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 8NC_000008.11:g.5724652T>C
GRCh37.p13 chr 8NC_000008.10:g.5582174T>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 )
chr855338925534065E081-48109
chr855342775534401E081-47773
chr855344105534570E081-47604
chr855345745534624E081-47550
chr855346725534726E081-47448
chr856164965616701E08134322
chr856168375616898E08134663
chr856170585617108E08134884

Mpgyi