rs6870671

Homo sapiens
T>C
None
Check p-value
SNV (Single Nucleotide Variation)
C=0058 (1751/29986,GnomAD)
C=0094 (2750/29118,TOPMED)
C=0063 (318/5008,1000G)
C=0001 (2/3854,ALSPAC)
C=0001 (2/3708,TWINSUK)
chr5:98303039 (GRCh38.p7) (5q15)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 5NC_000005.10:g.98303039T>C
GRCh37.p13 chr 5NC_000005.9:g.97638743T>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 )
chr59763728697637608E067-1135
chr59764480997644936E0686066
chr59765603597656120E06817292
chr59765615697656337E06817413
chr59765603597656120E06917292
chr59765615697656337E06917413
chr59763728697637608E071-1135
chr59765102297651072E07112279
chr59765112997651210E07112386
chr59764997797650529E07211234
chr59765102297651072E07212279
chr59765112997651210E07212386
chr59763728697637608E074-1135
chr59764480997644936E0746066
chr59765603597656120E07417292
chr59765615697656337E07417413






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