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rs1064797046

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome13
Position50948073
GeneRNASEH2B
is asnp
is mentioned by
dbSNPrs1064797046
dbSNP (old)rs1064797046
ClinGenrs1064797046
ebirs1064797046
HLIrs1064797046
Exacrs1064797046
Gnomadrs1064797046
Varsomers1064797046
Maprs1064797046
PheGenIrs1064797046
Biobankrs1064797046
1000 genomesrs1064797046
hgdprs1064797046
ensemblrs1064797046
gopubmedrs1064797046
geneviewrs1064797046
scholarrs1064797046
googlers1064797046
pharmgkbrs1064797046
gwascentralrs1064797046
openSNPrs1064797046
23andMers1064797046
23andMe allrs1064797046
SNPshotrs1064797046
SNPdbers1064797046
MSV3drs1064797046
GWAS Ctlgrs1064797046
Max Magnitude0
ClinVar
Risk rs1064797046(A;A)
Alt rs1064797046(A;A)
Reference Rs1064797046(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RNASEH2B
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.51522209G>A
CLNSRC
CLNACC RCV000486862.1,