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rs730881774

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881774(-;-)
Make rs730881774(-;A)
Make rs730881774(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47429822
GeneMSH2
is asnp
is mentioned by
dbSNPrs730881774
ebirs730881774
HLIrs730881774
Exacrs730881774
Varsomers730881774
Maprs730881774
PheGenIrs730881774
hapmaprs730881774
1000 genomesrs730881774
hgdprs730881774
ensemblrs730881774
gopubmedrs730881774
geneviewrs730881774
scholarrs730881774
googlers730881774
pharmgkbrs730881774
gwascentralrs730881774
openSNPrs730881774
23andMers730881774
23andMe allrs730881774
SNP Nexus

SNPshotrs730881774
SNPdbers730881774
MSV3drs730881774
GWAS Ctlgrs730881774
Max Magnitude0
ClinVar
Risk rs730881774(A;A)
Alt rs730881774(A;A)
Reference rs730881774(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47656961dupA
CLNSRC
CLNACC RCV000160628.1,