rs9524600

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0136 (4077/29948,GnomAD)
G=0170 (4969/29118,TOPMED)
G=0132 (663/5008,1000G)
G=0104 (401/3854,ALSPAC)
G=0104 (384/3708,TWINSUK)
chr13:87105954 (GRCh38.p7) (13q31.2)
AD
GWASdb2
1   publication(s)
See rs on genome
9 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 13NC_000013.11:g.87105954A>G
GRCh37.p13 chr 13NC_000013.10:g.87758209A>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 )
chr138778075187780970E07022542
chr138778099087781070E07022781
chr138778113987781194E07022930
chr138778136187781523E07023152
chr138778160987781698E07023400
chr138778189787782225E07023688
chr138778224887782420E07024039
chr138778273087782844E07024521
chr138778399687784117E07025787

Mpgyi