rs1407862

Homo sapiens
G>A
KDM4C : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
A=0472 (14136/29894,GnomAD)
A=0472 (13770/29118,TOPMED)
G==0496 (2485/5008,1000G)
A=0453 (1747/3854,ALSPAC)
A=0462 (1714/3708,TWINSUK)
chr9:7032776 (GRCh38.p7) (9p24.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 9NC_000009.12:g.7032776G>A
GRCh37.p13 chr 9NC_000009.11:g.7032776G>A

Gene: KDM4C, lysine demethylase 4C(plus strand)

Molecule type Change Amino acid[Codon] SO Term
KDM4C transcript variant 3NM_001146695.1:c.N/AIntron Variant
KDM4C transcript variant 4NM_001146696.1:c.N/AIntron Variant
KDM4C transcript variant 5NM_001304339.1:c.N/AIntron Variant
KDM4C transcript variant 6NM_001304340.1:c.N/AIntron Variant
KDM4C transcript variant 1NM_015061.3:c.N/AIntron Variant
KDM4C transcript variant 7NM_001304341.1:c.N/AGenic Downstream Transcript Variant
KDM4C transcript variant 8NR_130707.1:n.N/AGenic Downstream Transcript Variant
KDM4C transcript variant X1XM_006716741.2:c.N/AIntron Variant
KDM4C transcript variant X4XM_011517811.2:c.N/AIntron Variant
KDM4C transcript variant X6XM_011517812.2:c.N/AIntron Variant
KDM4C transcript variant X14XM_011517816.2:c.N/AIntron Variant
KDM4C transcript variant X2XM_017014498.1:c.N/AIntron Variant
KDM4C transcript variant X3XM_017014499.1:c.N/AIntron Variant
KDM4C transcript variant X5XM_017014500.1:c.N/AIntron Variant
KDM4C transcript variant X7XM_017014501.1:c.N/AIntron Variant
KDM4C transcript variant X9XM_017014502.1:c.N/AIntron Variant
KDM4C transcript variant X13XM_017014503.1:c.N/AIntron Variant
KDM4C transcript variant X15XM_017014504.1:c.N/AIntron Variant
KDM4C transcript variant X16XM_017014505.1:c.N/AIntron Variant
KDM4C transcript variant X17XM_017014506.1:c.N/AIntron Variant
KDM4C transcript variant X8XR_001746252.1:n.N/AIntron Variant
KDM4C transcript variant X10XR_001746253.1:n.N/AIntron Variant
KDM4C transcript variant X11XR_001746254.1:n.N/AIntron Variant
KDM4C transcript variant X12XR_001746255.1:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.488A=0.512
1000GenomesAmericanSub694G=0.500A=0.500
1000GenomesEast AsianSub1008G=0.534A=0.466
1000GenomesEuropeSub1006G=0.579A=0.421
1000GenomesGlobalStudy-wide5008G=0.496A=0.504
1000GenomesSouth AsianSub978G=0.380A=0.620
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.547A=0.453
The Genome Aggregation DatabaseAfricanSub8698G=0.488A=0.512
The Genome Aggregation DatabaseAmericanSub838G=0.480A=0.520
The Genome Aggregation DatabaseEast AsianSub1610G=0.560A=0.440
The Genome Aggregation DatabaseEuropeSub18446G=0.543A=0.457
The Genome Aggregation DatabaseGlobalStudy-wide29894G=0.527A=0.472
The Genome Aggregation DatabaseOtherSub302G=0.640A=0.360
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.527A=0.472
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.538A=0.462
PMID Title Author Journal
22072270Genome-wide association study identifies 5q21 and 9p24.1 (KDM4C) loci associated with alcohol withdrawal symptoms.Wang KSJ Neural Transm (Vienna)

P-Value

SNP ID p-value Traits Study
rs14078624.93E-05alcohol withdrawal symptoms22072270

eQTL of rs1407862 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 rs1407862 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.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr970525037053138E06819727
chr970567667057012E06823990
chr970572237057335E06824447
chr970573427057422E06824566
chr970574577058000E06824681
chr970580907058230E06825314
chr970583107058379E06825534
chr970583887058453E06825612
chr970585007058568E06825724
chr970525037053138E06919727
chr970532467053364E06920470
chr970533777053446E06920601
chr970534847053547E06920708
chr970574577058000E06924681
chr970580907058230E06925314
chr970787967079177E06946020
chr970825617082720E06949785
chr970372737037323E0704497
chr970825617082720E07249785
chr970525037053138E07319727
chr970532467053364E07320470
chr970533777053446E07320601
chr969999917000124E074-32652
chr970563877056589E07423611
chr970567667057012E07423990
chr970574577058000E07424681
chr970787967079177E07446020
chr970525037053138E08119727
chr970532467053364E08120470
chr970533777053446E08120601
chr970532467053364E08220470
chr970533777053446E08220601
chr970550537055161E08222277