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rs797044565

From SNPedia

Orientationplus
Make rs797044565(-;-)
Make rs797044565(-;CAGT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position118503457
GeneKMT2A
is asnp
is mentioned by
dbSNPrs797044565
ebirs797044565
HLIrs797044565
Exacrs797044565
Varsomers797044565
Maprs797044565
PheGenIrs797044565
hapmaprs797044565
1000 genomesrs797044565
hgdprs797044565
ensemblrs797044565
gopubmedrs797044565
geneviewrs797044565
scholarrs797044565
googlers797044565
pharmgkbrs797044565
gwascentralrs797044565
openSNPrs797044565
23andMers797044565
23andMe allrs797044565
SNP Nexus

SNPshotrs797044565
SNPdbers797044565
MSV3drs797044565
GWAS Ctlgrs797044565
Max Magnitude
ClinVar
Risk rs797044565(;)
Alt rs797044565(;)
Reference rs797044565(CAGT;CAGT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118374172_118374175delCAGT
CLNSRC
CLNACC RCV000171465.1,