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rs121918546

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918546(A;G)
Make rs121918546(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position143041855
GeneARHGAP26
is asnp
is mentioned by
dbSNPrs121918546
ebirs121918546
HLIrs121918546
Exacrs121918546
Varsomers121918546
Maprs121918546
PheGenIrs121918546
hapmaprs121918546
1000 genomesrs121918546
hgdprs121918546
ensemblrs121918546
gopubmedrs121918546
geneviewrs121918546
scholarrs121918546
googlers121918546
pharmgkbrs121918546
gwascentralrs121918546
openSNPrs121918546
23andMers121918546
23andMe allrs121918546
SNP Nexus

SNPshotrs121918546
SNPdbers121918546
MSV3drs121918546
GWAS Ctlgrs121918546
Max Magnitude0
OMIM605370
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918546(C,G;C,G)
Alt rs121918546(C,G;C,G)
Reference rs121918546(A;A)
Significance Pathogenic
Disease Juvenile myelomonocytic leukemia
Variation info
Gene ARHGAP26
CLNDBN Juvenile myelomonocytic leukemia
Reversed 0
HGVS NC_000005.9:g.142421420A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005355.4,