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rs730881775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs730881775(-;A)
Make rs730881775(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47403202
GeneMSH2
is asnp
is mentioned by
dbSNPrs730881775
dbSNP (old)rs730881775
ClinGenrs730881775
ebirs730881775
HLIrs730881775
Exacrs730881775
Gnomadrs730881775
Varsomers730881775
Maprs730881775
PheGenIrs730881775
Biobankrs730881775
1000 genomesrs730881775
hgdprs730881775
ensemblrs730881775
gopubmedrs730881775
geneviewrs730881775
scholarrs730881775
googlers730881775
pharmgkbrs730881775
gwascentralrs730881775
openSNPrs730881775
23andMers730881775
23andMe allrs730881775
SNP Nexus

SNPshotrs730881775
SNPdbers730881775
MSV3drs730881775
GWAS Ctlgrs730881775
Max Magnitude0
ClinVar
Risk rs730881775(A;A)
Alt rs730881775(A;A)
Reference Rs730881775(-;-)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47630341dup; NC_000002.11:g.47630341dupA
CLNSRC
CLNACC RCV000491987.1, RCV000160630.2,