rs10975990

Homo sapiens
G>A
KDM4C : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G==0472 (14099/29850,GnomAD)
G==0473 (13798/29118,TOPMED)
G==0424 (2125/5008,1000G)
A=0489 (1884/3854,ALSPAC)
A=0499 (1851/3708,TWINSUK)
chr9:7026716 (GRCh38.p7) (9p24.1)
AD
GWASdb2
2   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 9NC_000009.12:g.7026716G>A
GRCh37.p13 chr 9NC_000009.11:g.7026716G>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=0.413A=0.587
1000GenomesAmericanSub694G=0.460A=0.540
1000GenomesEast AsianSub1008G=0.433A=0.567
1000GenomesEuropeSub1006G=0.551A=0.449
1000GenomesGlobalStudy-wide5008G=0.424A=0.576
1000GenomesSouth AsianSub978G=0.280A=0.720
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.511A=0.489
The Genome Aggregation DatabaseAfricanSub8682G=0.412A=0.588
The Genome Aggregation DatabaseAmericanSub834G=0.470A=0.530
The Genome Aggregation DatabaseEast AsianSub1600G=0.464A=0.536
The Genome Aggregation DatabaseEuropeSub18432G=0.499A=0.500
The Genome Aggregation DatabaseGlobalStudy-wide29850G=0.472A=0.527
The Genome Aggregation DatabaseOtherSub302G=0.620A=0.380
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.473A=0.526
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.501A=0.499
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)
25043041Neuropsychosocial profiles of current and future adolescent alcohol misusers.Whelan RNature

P-Value

SNP ID p-value Traits Study
rs109759907.15E-06alcohol withdrawal symptoms22072270

eQTL of rs10975990 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 rs10975990 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 )
chr969786416978691E067-48025
chr969787546978915E067-47801
chr970525037053138E06825787
chr970567667057012E06830050
chr970572237057335E06830507
chr970573427057422E06830626
chr970574577058000E06830741
chr970580907058230E06831374
chr970583107058379E06831594
chr970583887058453E06831672
chr970585007058568E06831784
chr970525037053138E06925787
chr970532467053364E06926530
chr970533777053446E06926661
chr970534847053547E06926768
chr970574577058000E06930741
chr970580907058230E06931374
chr970372737037323E07010557
chr969786416978691E071-48025
chr969787546978915E071-47801
chr970525037053138E07325787
chr970532467053364E07326530
chr970533777053446E07326661
chr969999917000124E074-26592
chr970563877056589E07429671
chr970567667057012E07430050
chr970574577058000E07430741
chr970525037053138E08125787
chr970532467053364E08126530
chr970533777053446E08126661
chr970532467053364E08226530
chr970533777053446E08226661
chr970550537055161E08228337