rs10758821

Homo sapiens
G>T
KDM4C : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
T=0437 (13063/29870,GnomAD)
T=0421 (12276/29118,TOPMED)
T=0465 (2331/5008,1000G)
T=0451 (1738/3854,ALSPAC)
T=0461 (1710/3708,TWINSUK)
chr9:7030268 (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.7030268G>T
GRCh37.p13 chr 9NC_000009.11:g.7030268G>T

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=0.618T=0.382
1000GenomesAmericanSub694G=0.510T=0.490
1000GenomesEast AsianSub1008G=0.539T=0.461
1000GenomesEuropeSub1006G=0.582T=0.418
1000GenomesGlobalStudy-wide5008G=0.535T=0.465
1000GenomesSouth AsianSub978G=0.390T=0.610
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.549T=0.451
The Genome Aggregation DatabaseAfricanSub8688G=0.595T=0.405
The Genome Aggregation DatabaseAmericanSub830G=0.490T=0.510
The Genome Aggregation DatabaseEast AsianSub1602G=0.561T=0.439
The Genome Aggregation DatabaseEuropeSub18448G=0.549T=0.450
The Genome Aggregation DatabaseGlobalStudy-wide29870G=0.562T=0.437
The Genome Aggregation DatabaseOtherSub302G=0.640T=0.360
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.578T=0.421
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.539T=0.461
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
rs107588212.79E-05alcohol withdrawal symptoms22072270

eQTL of rs10758821 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 rs10758821 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 )
chr970525037053138E06822235
chr970567667057012E06826498
chr970572237057335E06826955
chr970573427057422E06827074
chr970574577058000E06827189
chr970580907058230E06827822
chr970583107058379E06828042
chr970583887058453E06828120
chr970585007058568E06828232
chr970525037053138E06922235
chr970532467053364E06922978
chr970533777053446E06923109
chr970534847053547E06923216
chr970574577058000E06927189
chr970580907058230E06927822
chr970787967079177E06948528
chr970372737037323E0707005
chr970525037053138E07322235
chr970532467053364E07322978
chr970533777053446E07323109
chr969999917000124E074-30144
chr970563877056589E07426119
chr970567667057012E07426498
chr970574577058000E07427189
chr970787967079177E07448528
chr970525037053138E08122235
chr970532467053364E08122978
chr970533777053446E08123109
chr970532467053364E08222978
chr970533777053446E08223109
chr970550537055161E08224785