rs7034275

Homo sapiens
G>C
KDM4C : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
C=0410 (12291/29932,GnomAD)
C=0358 (10448/29118,TOPMED)
C=0286 (1434/5008,1000G)
C=0460 (1771/3854,ALSPAC)
C=0449 (1664/3708,TWINSUK)
chr9:7067344 (GRCh38.p7) (9p24.1)
ND
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 9NC_000009.12:g.7067344G>C
GRCh37.p13 chr 9NC_000009.11:g.7067344G>C

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 X13XM_017014503.1: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 X9XM_017014502.1:c.N/AGenic Downstream Transcript Variant
KDM4C transcript variant X15XM_017014504.1:c.N/AGenic Downstream Transcript 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

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 )
chr970525037053138E068-14206
chr970567667057012E068-10332
chr970572237057335E068-10009
chr970573427057422E068-9922
chr970574577058000E068-9344
chr970580907058230E068-9114
chr970583107058379E068-8965
chr970583887058453E068-8891
chr970585007058568E068-8776
chr970852027085252E06817858
chr970853617085412E06818017
chr970525037053138E069-14206
chr970532467053364E069-13980
chr970533777053446E069-13898
chr970534847053547E069-13797
chr970574577058000E069-9344
chr970580907058230E069-9114
chr970787967079177E06911452
chr970825617082720E06915217
chr970852027085252E06917858
chr970853617085412E06918017
chr970881537088231E06920809
chr970883017088405E06920957
chr970372737037323E070-30021
chr970847897084843E07117445
chr970852027085252E07117858
chr970853617085412E07118017
chr970825617082720E07215217
chr970525037053138E073-14206
chr970532467053364E073-13980
chr970533777053446E073-13898
chr970563877056589E074-10755
chr970567667057012E074-10332
chr970574577058000E074-9344
chr970787967079177E07411452
chr970847897084843E07417445
chr970852027085252E07417858
chr970853617085412E07418017
chr971157467115884E07448402
chr970525037053138E081-14206
chr970532467053364E081-13980
chr970533777053446E081-13898
chr970532467053364E082-13980
chr970533777053446E082-13898
chr970550537055161E082-12183
chr970885017089004E08221157
chr970892027089715E08221858









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