rs10512096

Homo sapiens
T>C
None
Check p-value
SNV (Single Nucleotide Variation)
T==0308 (9219/29920,GnomAD)
T==0343 (9989/29118,TOPMED)
T==0253 (1266/5008,1000G)
T==0288 (1111/3854,ALSPAC)
T==0282 (1047/3708,TWINSUK)
chr9:80115418 (GRCh38.p7) (9q21.31)
AD
GWASdb2
1   publication(s)
See rs on genome
9 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 9NC_000009.12:g.80115418T>C
GRCh37.p13 chr 9NC_000009.11:g.82730333T>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 )
chr98277356582774172E06843232
chr98277177482773115E07041441
chr98277316182773374E07042828
chr98277338882773483E07043055
chr98277356582774172E07043232
chr98277177482773115E08241441
chr98277316182773374E08242828
chr98277338882773483E08243055
chr98277356582774172E08243232



Mpgyi