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rs541623924

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs541623924(-;-)
Make rs541623924(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47475272
GeneMSH2
is asnp
is mentioned by
dbSNPrs541623924
ebirs541623924
HLIrs541623924
Exacrs541623924
Varsomers541623924
Maprs541623924
PheGenIrs541623924
hapmaprs541623924
1000 genomesrs541623924
hgdprs541623924
ensemblrs541623924
gopubmedrs541623924
geneviewrs541623924
scholarrs541623924
googlers541623924
pharmgkbrs541623924
gwascentralrs541623924
openSNPrs541623924
23andMers541623924
23andMe allrs541623924
SNP Nexus

SNPshotrs541623924
SNPdbers541623924
MSV3drs541623924
GWAS Ctlgrs541623924
Max Magnitude0
ClinVar
Risk rs541623924(TA,TT;TA,TT)
Alt rs541623924(TA,TT;TA,TT)
Reference rs541623924(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47702411dupT
CLNSRC
CLNACC RCV000202039.1,