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rs63749929

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(I;I) 0
Make rs63749929(-;-)
Make rs63749929(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475251
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749929
ebirs63749929
HLIrs63749929
Exacrs63749929
Varsomers63749929
Maprs63749929
PheGenIrs63749929
hapmaprs63749929
1000 genomesrs63749929
hgdprs63749929
ensemblrs63749929
gopubmedrs63749929
geneviewrs63749929
scholarrs63749929
googlers63749929
pharmgkbrs63749929
gwascentralrs63749929
openSNPrs63749929
23andMers63749929
23andMe allrs63749929
SNP Nexus

SNPshotrs63749929
SNPdbers63749929
MSV3drs63749929
GWAS Ctlgrs63749929
Max Magnitude0
ClinVar
Risk rs63749929(;)
Alt rs63749929(;)
Reference rs63749929(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702390delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076332.2,