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rs63749991

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63749991(C;G)
Make rs63749991(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position47414318
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749991
ebirs63749991
HLIrs63749991
Exacrs63749991
Varsomers63749991
Maprs63749991
PheGenIrs63749991
hapmaprs63749991
1000 genomesrs63749991
hgdprs63749991
ensemblrs63749991
gopubmedrs63749991
geneviewrs63749991
scholarrs63749991
googlers63749991
pharmgkbrs63749991
gwascentralrs63749991
openSNPrs63749991
23andMers63749991
23andMe allrs63749991
SNP Nexus

SNPshotrs63749991
SNPdbers63749991
MSV3drs63749991
GWAS Ctlgrs63749991
Max Magnitude0
ClinVar
Risk rs63749991(A,G;A,G)
Alt rs63749991(A,G;A,G)
Reference rs63749991(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641457C>A; NC_000002.11:g.47641457C>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076734.2, RCV000205315.1,