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rs370376334

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs370376334(C;C)
Make rs370376334(C;G)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position25244599
GeneDNMT3A
is asnp
is mentioned by
dbSNPrs370376334
dbSNP (classic)rs370376334
ClinGenrs370376334
ebirs370376334
HLIrs370376334
Exacrs370376334
Gnomadrs370376334
Varsomers370376334
LitVarrs370376334
Maprs370376334
PheGenIrs370376334
Biobankrs370376334
1000 genomesrs370376334
hgdprs370376334
ensemblrs370376334
geneviewrs370376334
scholarrs370376334
googlers370376334
pharmgkbrs370376334
gwascentralrs370376334
openSNPrs370376334
23andMers370376334
SNPshotrs370376334
SNPdbers370376334
MSV3drs370376334
GWAS Ctlgrs370376334
Max Magnitude0
ClinVar
Risk rs370376334(C;C)
Alt rs370376334(C;C)
Reference Rs370376334(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DNMT3A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.25467468G>C
CLNSRC
CLNACC RCV000304967.1,