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rs1057520788

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520788(C;C)
Make rs1057520788(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position25244322
GeneDNMT3A
is asnp
is mentioned by
dbSNPrs1057520788
dbSNP (old)rs1057520788
ClinGenrs1057520788
ebirs1057520788
HLIrs1057520788
Exacrs1057520788
Gnomadrs1057520788
Varsomers1057520788
Maprs1057520788
PheGenIrs1057520788
Biobankrs1057520788
1000 genomesrs1057520788
hgdprs1057520788
ensemblrs1057520788
gopubmedrs1057520788
geneviewrs1057520788
scholarrs1057520788
googlers1057520788
pharmgkbrs1057520788
gwascentralrs1057520788
openSNPrs1057520788
23andMers1057520788
23andMe allrs1057520788
SNPshotrs1057520788
SNPdbers1057520788
MSV3drs1057520788
GWAS Ctlgrs1057520788
Max Magnitude0
ClinVar
Risk rs1057520788(C;C)
Alt rs1057520788(C;C)
Reference Rs1057520788(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DNMT3A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.25467191A>G
CLNSRC
CLNACC RCV000439792.1,