rs6583832

Homo sapiens
T>G
KIF11 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G=0144 (4315/29964,GnomAD)
G=0216 (6315/29118,TOPMED)
G=0178 (892/5008,1000G)
G=0041 (159/3854,ALSPAC)
G=0038 (141/3708,TWINSUK)
chr10:92641615 (GRCh38.p7) (10q23.33)
ND
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 10NC_000010.11:g.92641615T>G
GRCh37.p13 chr 10NC_000010.10:g.94401372T>G
KIF11 RefSeqGeneNG_032580.1:g.53548T>G

Gene: KIF11, kinesin family member 11(plus strand)

Molecule type Change Amino acid[Codon] SO Term
KIF11 transcriptNM_004523.3:c.N/AIntron Variant

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.

Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr109435222694354210E067-47162
chr109435222694354210E068-47162
chr109435222694354210E069-47162
chr109435222694354210E070-47162
chr109435441594354540E070-46832
chr109435455594354945E070-46427
chr109435516794355256E070-46116
chr109435222694354210E071-47162
chr109435222694354210E072-47162
chr109435222694354210E073-47162
chr109435222694354210E074-47162
chr109435222694354210E081-47162
chr109435222694354210E082-47162
chr109435441594354540E082-46832
chr109435455594354945E082-46427










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