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rs63749814

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63749814(-;-)
Make rs63749814(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429773
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749814
ebirs63749814
HLIrs63749814
Exacrs63749814
Varsomers63749814
Maprs63749814
PheGenIrs63749814
hapmaprs63749814
1000 genomesrs63749814
hgdprs63749814
ensemblrs63749814
gopubmedrs63749814
geneviewrs63749814
scholarrs63749814
googlers63749814
pharmgkbrs63749814
gwascentralrs63749814
openSNPrs63749814
23andMers63749814
23andMe allrs63749814
SNP Nexus

SNPshotrs63749814
SNPdbers63749814
MSV3drs63749814
GWAS Ctlgrs63749814
Max Magnitude0
ClinVar
Risk rs63749814(;)
Alt rs63749814(;)
Reference rs63749814(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47656912delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076040.2,