rs372255102

Homo sapiens
T>C
None
Check p-value
SNV (Single Nucleotide Variation)
T==0468 (2342/5008,1000G)
chr21:26630728 (GRCh38.p7) (21q21.3)
AD
GWASCatalog
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 21NC_000021.9:g.26630728T>C
GRCh37.p13 chr 21NC_000021.8:g.28003047T>C

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322T=0.778C=0.222
1000GenomesAmericanSub694T=0.450C=0.550
1000GenomesEast AsianSub1008T=0.315C=0.685
1000GenomesEuropeSub1006T=0.329C=0.671
1000GenomesGlobalStudy-wide5008T=0.468C=0.532
1000GenomesSouth AsianSub978T=0.360C=0.640
PMID Title Author Journal
28040410A genome wide association study of fast beta EEG in families of European ancestry.Meyers JLInt J Psychophysiol

P-Value

SNP ID p-value Traits Study
rs3722551025E-07alcohol dependence28040410

eQTL of rs372255102 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
There is no eQTL annotation for this SNP

meQTL of rs372255102 in Fetal Brain

Probe ID Position Gene beta p-value
There is no meQTL annotation for this SNP

Genomic View

Chromatin Interaction

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