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rs63750933

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(I;I) 0
Make rs63750933(-;-)
Make rs63750933(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410240
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750933
ebirs63750933
HLIrs63750933
Exacrs63750933
Varsomers63750933
Maprs63750933
PheGenIrs63750933
hapmaprs63750933
1000 genomesrs63750933
hgdprs63750933
ensemblrs63750933
gopubmedrs63750933
geneviewrs63750933
scholarrs63750933
googlers63750933
pharmgkbrs63750933
gwascentralrs63750933
openSNPrs63750933
23andMers63750933
23andMe allrs63750933
SNP Nexus

SNPshotrs63750933
SNPdbers63750933
MSV3drs63750933
GWAS Ctlgrs63750933
Max Magnitude0
ClinVar
Risk rs63750933(;)
Alt rs63750933(;)
Reference rs63750933(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637379delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076624.2,