rs17028615

Homo sapiens
A>G
LOC100507053 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G=0063 (1888/29990,GnomAD)
G=0103 (2998/29118,TOPMED)
G=0063 (317/5008,1000G)
G=0001 (3/3854,ALSPAC)
G=0001 (2/3708,TWINSUK)
chr4:99150767 (GRCh38.p7) (4q23)
AD
GWASCatalog
2   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.99150767A>G
GRCh37.p13 chr 4NC_000004.11:g.100071924A>G

Gene: LOC100507053, uncharacterized LOC100507053(plus strand)

Molecule type Change Amino acid[Codon] SO Term
LOC100507053 transcriptNR_037884.1:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.775G=0.225
1000GenomesAmericanSub694A=0.970G=0.030
1000GenomesEast AsianSub1008A=1.000G=0.000
1000GenomesEuropeSub1006A=0.999G=0.001
1000GenomesGlobalStudy-wide5008A=0.937G=0.063
1000GenomesSouth AsianSub978A=1.000G=0.000
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.999G=0.001
The Genome Aggregation DatabaseAfricanSub8724A=0.786G=0.214
The Genome Aggregation DatabaseAmericanSub838A=0.990G=0.010
The Genome Aggregation DatabaseEast AsianSub1622A=1.000G=0.000
The Genome Aggregation DatabaseEuropeSub18504A=0.999G=0.000
The Genome Aggregation DatabaseGlobalStudy-wide29990A=0.937G=0.063
The Genome Aggregation DatabaseOtherSub302A=1.000G=0.000
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.897G=0.103
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.999G=0.001
PMID Title Author Journal
24166409Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci.Gelernter JMol Psychiatry
24625756Genetic determinants influencing human serum metabolome among African Americans.Yu BPLoS Genet

P-Value

SNP ID p-value Traits Study
rs170286151.00E-10alcohol dependence24166409
rs170286153.00E-08alcohol dependence24166409
rs170286156.00E-08alcohol dependence24166409

eQTL of rs17028615 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 rs17028615 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.