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rs63750896

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(T;T) 0 common in clinvar
Make rs63750896(-;-)
Make rs63750896(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478366
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750896
ebirs63750896
HLIrs63750896
Exacrs63750896
Varsomers63750896
Maprs63750896
PheGenIrs63750896
hapmaprs63750896
1000 genomesrs63750896
hgdprs63750896
ensemblrs63750896
gopubmedrs63750896
geneviewrs63750896
scholarrs63750896
googlers63750896
pharmgkbrs63750896
gwascentralrs63750896
openSNPrs63750896
23andMers63750896
23andMe allrs63750896
SNP Nexus

SNPshotrs63750896
SNPdbers63750896
MSV3drs63750896
GWAS Ctlgrs63750896
Max Magnitude0
ClinVar
Risk rs63750896(;)
Alt rs63750896(;)
Reference rs63750896(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705505delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076456.2,