Have questions? Visit https://www.reddit.com/r/SNPedia

rs797044937

From SNPedia

Orientationplus
Make rs797044937(-;-)
Make rs797044937(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position118473027
GeneKMT2A
is asnp
is mentioned by
dbSNPrs797044937
ebirs797044937
HLIrs797044937
Exacrs797044937
Varsomers797044937
Maprs797044937
PheGenIrs797044937
hapmaprs797044937
1000 genomesrs797044937
hgdprs797044937
ensemblrs797044937
gopubmedrs797044937
geneviewrs797044937
scholarrs797044937
googlers797044937
pharmgkbrs797044937
gwascentralrs797044937
openSNPrs797044937
23andMers797044937
23andMe allrs797044937
SNP Nexus

SNPshotrs797044937
SNPdbers797044937
MSV3drs797044937
GWAS Ctlgrs797044937
Max Magnitude
ClinVar
Risk rs797044937(;)
Alt rs797044937(;)
Reference rs797044937(A;A)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene KMT2A
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000011.9:g.118343742delA
CLNSRC
CLNACC RCV000190780.1,