rs2108831

Homo sapiens
G>C / G>T
None
Check p-value
SNV (Single Nucleotide Variation)
G==0168 (5050/29958,GnomAD)
G==0224 (6532/29118,TOPMED)
G==0182 (910/5008,1000G)
G==0064 (246/3854,ALSPAC)
G==0057 (210/3708,TWINSUK)
chr17:56640543 (GRCh38.p7) (17q22)
CD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 17NC_000017.11:g.56640543G>C
GRCh38.p7 chr 17NC_000017.11:g.56640543G>T
GRCh37.p13 chr 17NC_000017.10:g.54717904G>C
GRCh37.p13 chr 17NC_000017.10:g.54717904G>T

Genomic View

Chromatin Interaction

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