rs13134142

Homo sapiens
T>G
CCSER1 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G=0057 (1715/29878,GnomAD)
G=0049 (1444/29118,TOPMED)
G=0064 (320/5008,1000G)
G=0100 (386/3854,ALSPAC)
G=0098 (363/3708,TWINSUK)
chr4:90721760 (GRCh38.p7) (4q22.1)
AD
GWASdb2
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.90721760T>G
GRCh37.p13 chr 4NC_000004.11:g.91642911T>G

Gene: CCSER1, coiled-coil serine rich protein 1(plus strand)

Molecule type Change Amino acid[Codon] SO Term
CCSER1 transcript variant 1NM_001145065.1:c.N/AIntron Variant
CCSER1 transcript variant 2NM_207491.2:c.N/AIntron Variant
CCSER1 transcript variant X1XM_011531936.1:c.N/AIntron Variant
CCSER1 transcript variant X3XM_011531937.2:c.N/AIntron Variant
CCSER1 transcript variant X2XM_011531938.2:c.N/AIntron Variant
CCSER1 transcript variant X4XM_011531939.2:c.N/AIntron Variant
CCSER1 transcript variant X6XM_011531941.2:c.N/AIntron Variant
CCSER1 transcript variant X7XM_011531942.2:c.N/AIntron Variant
CCSER1 transcript variant X8XM_011531943.2:c.N/AIntron Variant
CCSER1 transcript variant X10XM_011531945.1:c.N/AIntron Variant
CCSER1 transcript variant X11XM_011531946.2:c.N/AIntron Variant
CCSER1 transcript variant X12XM_011531947.2:c.N/AIntron Variant
CCSER1 transcript variant X14XM_011531948.1:c.N/AIntron Variant
CCSER1 transcript variant X17XM_011531949.2:c.N/AIntron Variant
CCSER1 transcript variant X19XM_011531950.2:c.N/AIntron Variant
CCSER1 transcript variant X18XM_011531951.2:c.N/AIntron Variant
CCSER1 transcript variant X24XM_011531955.2:c.N/AIntron Variant
CCSER1 transcript variant X25XM_011531956.2:c.N/AIntron Variant
CCSER1 transcript variant X27XM_011531957.2:c.N/AIntron Variant
CCSER1 transcript variant X28XM_011531958.2:c.N/AIntron Variant
CCSER1 transcript variant X5XM_017008194.1:c.N/AIntron Variant
CCSER1 transcript variant X9XM_017008195.1:c.N/AIntron Variant
CCSER1 transcript variant X20XM_017008196.1:c.N/AIntron Variant
CCSER1 transcript variant X21XM_017008197.1:c.N/AIntron Variant
CCSER1 transcript variant X22XM_017008198.1:c.N/AIntron Variant
CCSER1 transcript variant X26XM_017008199.1:c.N/AIntron Variant
CCSER1 transcript variant X29XM_017008200.1:c.N/AGenic Downstream Transcript Variant
CCSER1 transcript variant X30XM_017008201.1:c.N/AGenic Downstream Transcript Variant
CCSER1 transcript variant X31XM_017008202.1:c.N/AGenic Downstream Transcript Variant
CCSER1 transcript variant X13XR_001741218.1:n.N/AIntron Variant
CCSER1 transcript variant X15XR_938733.2:n.N/AIntron Variant
CCSER1 transcript variant X16XR_938734.2:n.N/AIntron Variant
CCSER1 transcript variant X23XR_938735.2:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322T=0.998G=0.002
1000GenomesAmericanSub694T=0.950G=0.050
1000GenomesEast AsianSub1008T=0.978G=0.022
1000GenomesEuropeSub1006T=0.886G=0.114
1000GenomesGlobalStudy-wide5008T=0.936G=0.064
1000GenomesSouth AsianSub978T=0.850G=0.150
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854T=0.900G=0.100
The Genome Aggregation DatabaseAfricanSub8716T=0.984G=0.016
The Genome Aggregation DatabaseAmericanSub836T=0.970G=0.030
The Genome Aggregation DatabaseEast AsianSub1616T=0.969G=0.031
The Genome Aggregation DatabaseEuropeSub18408T=0.919G=0.080
The Genome Aggregation DatabaseGlobalStudy-wide29878T=0.942G=0.057
The Genome Aggregation DatabaseOtherSub302T=0.920G=0.080
Trans-Omics for Precision MedicineGlobalStudy-wide29118T=0.950G=0.049
UK 10K study - TwinsTWIN COHORTStudy-wide3708T=0.902G=0.098
PMID Title Author Journal
19581569Genome-wide association study of alcohol dependence.Treutlein JArch Gen Psychiatry

P-Value

SNP ID p-value Traits Study
rs131341423.67E-05alcohol dependence19581569

eQTL of rs13134142 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 rs13134142 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.