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rs1057518176

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518176(-;T)
Make rs1057518176(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position32787359
GeneDNMT3B
is asnp
is mentioned by
dbSNPrs1057518176
dbSNP (old)rs1057518176
ClinGenrs1057518176
ebirs1057518176
HLIrs1057518176
Exacrs1057518176
Gnomadrs1057518176
Varsomers1057518176
Maprs1057518176
PheGenIrs1057518176
Biobankrs1057518176
1000 genomesrs1057518176
hgdprs1057518176
ensemblrs1057518176
gopubmedrs1057518176
geneviewrs1057518176
scholarrs1057518176
googlers1057518176
pharmgkbrs1057518176
gwascentralrs1057518176
openSNPrs1057518176
23andMers1057518176
23andMe allrs1057518176
SNPshotrs1057518176
SNPdbers1057518176
MSV3drs1057518176
GWAS Ctlgrs1057518176
Max Magnitude0
ClinVar
Risk rs1057518176(T;T)
Alt rs1057518176(T;T)
Reference Rs1057518176(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene DNMT3B
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.31375165dupT
CLNSRC
CLNACC RCV000413388.1,