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rs63750069

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750069(-;-)
Make rs63750069(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410245
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750069
ebirs63750069
HLIrs63750069
Exacrs63750069
Varsomers63750069
Maprs63750069
PheGenIrs63750069
hapmaprs63750069
1000 genomesrs63750069
hgdprs63750069
ensemblrs63750069
gopubmedrs63750069
geneviewrs63750069
scholarrs63750069
googlers63750069
pharmgkbrs63750069
gwascentralrs63750069
openSNPrs63750069
23andMers63750069
23andMe allrs63750069
SNP Nexus

SNPshotrs63750069
SNPdbers63750069
MSV3drs63750069
GWAS Ctlgrs63750069
Max Magnitude0
ClinVar
Risk rs63750069(;)
Alt rs63750069(;)
Reference rs63750069(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637384delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076627.2,