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rs1057522023

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057522023(C;T)
Make rs1057522023(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position152148810
GeneKMT2C
is asnp
is mentioned by
dbSNPrs1057522023
dbSNP (old)rs1057522023
ClinGenrs1057522023
ebirs1057522023
HLIrs1057522023
Exacrs1057522023
Gnomadrs1057522023
Varsomers1057522023
Maprs1057522023
PheGenIrs1057522023
Biobankrs1057522023
1000 genomesrs1057522023
hgdprs1057522023
ensemblrs1057522023
gopubmedrs1057522023
geneviewrs1057522023
scholarrs1057522023
googlers1057522023
pharmgkbrs1057522023
gwascentralrs1057522023
openSNPrs1057522023
23andMers1057522023
23andMe allrs1057522023
SNPshotrs1057522023
SNPdbers1057522023
MSV3drs1057522023
GWAS Ctlgrs1057522023
Max Magnitude0
ClinVar
Risk rs1057522023(T;T)
Alt rs1057522023(T;T)
Reference Rs1057522023(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2C
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.151845895G>A
CLNSRC
CLNACC RCV000419858.1,