rs712013

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
G==0107 (3217/29928,GnomAD)
G==0128 (3748/29118,TOPMED)
G==0174 (871/5008,1000G)
G==0071 (273/3854,ALSPAC)
G==0059 (219/3708,TWINSUK)
chr7:52544575 (GRCh38.p7) (7p12.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 7NC_000007.14:g.52544575G>A
GRCh37.p13 chr 7NC_000007.13:g.52612271G>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 )
chr75256956652569649E067-42622
chr75256994252570054E067-42217
chr75257013752570192E067-42079
chr75256956652569649E070-42622
chr75256994252570054E070-42217
chr75257013752570192E070-42079
chr75263822652638400E08125955
chr75263850452639271E08126233
chr75263940152639520E08127130
chr75263958552639661E08127314
chr75263971152639772E08127440
chr75263989652639964E08127625
chr75264017952640333E08127908
chr75264098952641039E08128718



Mpgyi