rs2666055

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
G==0100 (3004/29946,GnomAD)
G==0107 (3143/29118,TOPMED)
G==0092 (463/5008,1000G)
G==0119 (458/3854,ALSPAC)
G==0119 (441/3708,TWINSUK)
chr4:178423266 (GRCh38.p7) (4q34.3)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 4NC_000004.12:g.178423266G>A
GRCh37.p13 chr 4NC_000004.11:g.179344420G>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 )
chr4179389460179389521E06745040
chr4179389563179389632E06745143
chr4179389710179389798E06745290
chr4179388979179389147E06944559
chr4179389460179389521E06945040
chr4179389563179389632E06945143
chr4179389710179389798E06945290
chr4179390172179390243E06945752
chr4179388979179389147E07144559
chr4179389460179389521E07145040
chr4179389563179389632E07145143
chr4179389710179389798E07145290
chr4179390172179390243E07145752
chr4179389460179389521E07245040
chr4179389563179389632E07245143
chr4179389710179389798E07245290
chr4179389460179389521E07445040
chr4179389563179389632E07445143
chr4179389710179389798E07445290
chr4179392252179392426E08247832






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