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rs63750644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(I;I) 0
Make rs63750644(-;-)
Make rs63750644(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47403336
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750644
ebirs63750644
HLIrs63750644
Exacrs63750644
Varsomers63750644
Maprs63750644
PheGenIrs63750644
hapmaprs63750644
1000 genomesrs63750644
hgdprs63750644
ensemblrs63750644
gopubmedrs63750644
geneviewrs63750644
scholarrs63750644
googlers63750644
pharmgkbrs63750644
gwascentralrs63750644
openSNPrs63750644
23andMers63750644
23andMe allrs63750644
SNP Nexus

SNPshotrs63750644
SNPdbers63750644
MSV3drs63750644
GWAS Ctlgrs63750644
Max Magnitude0
ClinVar
Risk rs63750644(;)
Alt rs63750644(;)
Reference rs63750644(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630475delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076169.2,