rs4837362

Homo sapiens
A>C / A>T
None
Check p-value
SNV (Single Nucleotide Variation)
A==0200 (5951/29748,GnomAD)
A==0214 (6252/29118,TOPMED)
A==0221 (1105/5008,1000G)
A==0234 (902/3854,ALSPAC)
A==0248 (920/3708,TWINSUK)
chr9:129400975 (GRCh38.p7) (9q34.11)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 9NC_000009.12:g.129400975A>C
GRCh38.p7 chr 9NC_000009.12:g.129400975A>T
GRCh37.p13 chr 9NC_000009.11:g.132163254A>C
GRCh37.p13 chr 9NC_000009.11:g.132163254A>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 )
chr93033307930333191E06720497
chr93033332030333400E06720738
chr93036057030360610E06747988
chr93036082530360905E06748243
chr93033307930333191E06920497
chr93033332030333400E06920738
chr93033293230333000E07120350
chr93033307930333191E07120497
chr93033293230333000E07220350
chr93033307930333191E07220497
chr93036057030360610E07447988
chr93036082530360905E07448243





Mpgyi