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rs149095705

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149095705(A;A)
Make rs149095705(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position25234307
GeneDNMT3A
is asnp
is mentioned by
dbSNPrs149095705
dbSNP (old)rs149095705
ClinGenrs149095705
ebirs149095705
HLIrs149095705
Exacrs149095705
Gnomadrs149095705
Varsomers149095705
LitVarrs149095705
Maprs149095705
PheGenIrs149095705
Biobankrs149095705
1000 genomesrs149095705
hgdprs149095705
ensemblrs149095705
gopubmedrs149095705
geneviewrs149095705
scholarrs149095705
googlers149095705
pharmgkbrs149095705
gwascentralrs149095705
openSNPrs149095705
23andMers149095705
23andMe allrs149095705
SNPshotrs149095705
SNPdbers149095705
MSV3drs149095705
GWAS Ctlgrs149095705
Max Magnitude0
ClinVar
Risk rs149095705(A;A) rs149095705(C;C) rs149095705(T;T)
Alt rs149095705(A;A) rs149095705(C;C) rs149095705(T;T)
Reference Rs149095705(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DNMT3A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.25457176G>A
CLNSRC
CLNACC RCV000413992.1,