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rs767226511

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs767226511(A;A)
Make rs767226511(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position25244579
GeneDNMT3A
is asnp
is mentioned by
dbSNPrs767226511
dbSNP (classic)rs767226511
ClinGenrs767226511
ebirs767226511
HLIrs767226511
Exacrs767226511
Gnomadrs767226511
Varsomers767226511
LitVarrs767226511
Maprs767226511
PheGenIrs767226511
Biobankrs767226511
1000 genomesrs767226511
hgdprs767226511
ensemblrs767226511
geneviewrs767226511
scholarrs767226511
googlers767226511
pharmgkbrs767226511
gwascentralrs767226511
openSNPrs767226511
23andMers767226511
SNPshotrs767226511
SNPdbers767226511
MSV3drs767226511
GWAS Ctlgrs767226511
Max Magnitude0
ClinVar
Risk rs767226511(A;A) rs767226511(G;G) rs767226511(T;T)
Alt rs767226511(A;A) rs767226511(G;G) rs767226511(T;T)
Reference Rs767226511(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DNMT3A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.25467448C>T
CLNSRC
CLNACC RCV000486870.1,