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rs745714537

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs745714537(A;C)
Make rs745714537(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position25240411
GeneDNMT3A
is asnp
is mentioned by
dbSNPrs745714537
dbSNP (classic)rs745714537
ClinGenrs745714537
ebirs745714537
HLIrs745714537
Exacrs745714537
Gnomadrs745714537
Varsomers745714537
LitVarrs745714537
Maprs745714537
PheGenIrs745714537
Biobankrs745714537
1000 genomesrs745714537
hgdprs745714537
ensemblrs745714537
geneviewrs745714537
scholarrs745714537
googlers745714537
pharmgkbrs745714537
gwascentralrs745714537
openSNPrs745714537
23andMers745714537
SNPshotrs745714537
SNPdbers745714537
MSV3drs745714537
GWAS Ctlgrs745714537
Max Magnitude0
ClinVar
Risk rs745714537(C;C) rs745714537(T;T)
Alt rs745714537(C;C) rs745714537(T;T)
Reference Rs745714537(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DNMT3A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.25463280A>C
CLNSRC
CLNACC RCV000422670.1,