rs4129566

Homo sapiens
T>C
None
Check p-value
SNV (Single Nucleotide Variation)
C=0107 (3222/29966,GnomAD)
C=0112 (3286/29118,TOPMED)
C=0091 (458/5008,1000G)
C=0135 (520/3854,ALSPAC)
C=0144 (535/3708,TWINSUK)
chr4:173626006 (GRCh38.p7) (4q34.1)
CD
GWASdb2 | GWASCatalog
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 4NC_000004.12:g.173626006T>C
GRCh37.p13 chr 4NC_000004.11:g.174547157T>C

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.