rs3843552

Homo sapiens
G>A / G>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0127 (3808/29876,GnomAD)
T=0140 (4095/29118,TOPMED)
T=0174 (872/5008,1000G)
T=0060 (231/3854,ALSPAC)
T=0048 (178/3708,TWINSUK)
chr8:100801040 (GRCh38.p7) (8q22.3)
AD
GWASdb2
2   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 8NC_000008.11:g.100801040G>A
GRCh38.p7 chr 8NC_000008.11:g.100801040G>T
GRCh37.p13 chr 8NC_000008.10:g.101813268G>A
GRCh37.p13 chr 8NC_000008.10:g.101813268G>T

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 )
chr8101773554101775046E068-38132
chr8101847470101848214E06834292
chr8101764400101764498E071-48680
chr8101764560101764751E071-48427
chr8101764770101764823E071-48355
chr8101803597101803661E072-9517
chr8101803758101804338E074-8840
chr8101804391101804510E074-8668
chr8101847470101848214E07434292
chr8101848259101848339E07435081
chr8101859230101859295E07446052
chr8101775773101775823E081-37355
chr8101775832101775882E081-37296
chr8101775951101776079E081-37099
chr8101803597101803661E081-9517
chr8101803758101804338E081-8840
chr8101804391101804510E081-8668
chr8101851627101851825E08138449
chr8101851845101851917E08138667
chr8101775334101775644E082-37534






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