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rs730881776

From SNPedia

Orientationplus
Geno Mag Summary
(GCAT;GCAT) 0 common in clinvar
Make rs730881776(-;-)
Make rs730881776(-;ATGC)
Make rs730881776(ATGC;ATGC)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47475181
GeneMSH2
is asnp
is mentioned by
dbSNPrs730881776
ebirs730881776
HLIrs730881776
Exacrs730881776
Varsomers730881776
Maprs730881776
PheGenIrs730881776
hapmaprs730881776
1000 genomesrs730881776
hgdprs730881776
ensemblrs730881776
gopubmedrs730881776
geneviewrs730881776
scholarrs730881776
googlers730881776
pharmgkbrs730881776
gwascentralrs730881776
openSNPrs730881776
23andMers730881776
23andMe allrs730881776
SNP Nexus

SNPshotrs730881776
SNPdbers730881776
MSV3drs730881776
GWAS Ctlgrs730881776
Max Magnitude0
ClinVar
Risk rs730881776(;)
Alt rs730881776(;)
Reference rs730881776(GCAT;GCAT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47702320_47702323delATGC
CLNSRC
CLNACC RCV000160631.1,