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rs1057518093

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518093(A;A)
Make rs1057518093(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position152139792
GeneKMT2C
is asnp
is mentioned by
dbSNPrs1057518093
dbSNP (old)rs1057518093
ClinGenrs1057518093
ebirs1057518093
HLIrs1057518093
Exacrs1057518093
Gnomadrs1057518093
Varsomers1057518093
Maprs1057518093
PheGenIrs1057518093
Biobankrs1057518093
1000 genomesrs1057518093
hgdprs1057518093
ensemblrs1057518093
gopubmedrs1057518093
geneviewrs1057518093
scholarrs1057518093
googlers1057518093
pharmgkbrs1057518093
gwascentralrs1057518093
openSNPrs1057518093
23andMers1057518093
23andMe allrs1057518093
SNPshotrs1057518093
SNPdbers1057518093
MSV3drs1057518093
GWAS Ctlgrs1057518093
Max Magnitude0
ClinVar
Risk rs1057518093(A;A)
Alt rs1057518093(A;A)
Reference Rs1057518093(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2C
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.151836877C>T
CLNSRC
CLNACC RCV000414032.1,