Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057517815

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517815(A;G)
Make rs1057517815(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position50930675
GeneRNASEH2B
is asnp
is mentioned by
dbSNPrs1057517815
dbSNP (old)rs1057517815
ClinGenrs1057517815
ebirs1057517815
HLIrs1057517815
Exacrs1057517815
Gnomadrs1057517815
Varsomers1057517815
Maprs1057517815
PheGenIrs1057517815
Biobankrs1057517815
1000 genomesrs1057517815
hgdprs1057517815
ensemblrs1057517815
gopubmedrs1057517815
geneviewrs1057517815
scholarrs1057517815
googlers1057517815
pharmgkbrs1057517815
gwascentralrs1057517815
openSNPrs1057517815
23andMers1057517815
23andMe allrs1057517815
SNP Nexus

SNPshotrs1057517815
SNPdbers1057517815
MSV3drs1057517815
GWAS Ctlgrs1057517815
Max Magnitude0
ClinVar
Risk rs1057517815(G;G)
Alt rs1057517815(G;G)
Reference Rs1057517815(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RNASEH2B
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.51504811A>G
CLNSRC
CLNACC RCV000414685.1,