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rs63750572

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750572(-;-)
Make rs63750572(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476565
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750572
ebirs63750572
HLIrs63750572
Exacrs63750572
Varsomers63750572
Maprs63750572
PheGenIrs63750572
hapmaprs63750572
1000 genomesrs63750572
hgdprs63750572
ensemblrs63750572
gopubmedrs63750572
geneviewrs63750572
scholarrs63750572
googlers63750572
pharmgkbrs63750572
gwascentralrs63750572
openSNPrs63750572
23andMers63750572
23andMe allrs63750572
SNP Nexus

SNPshotrs63750572
SNPdbers63750572
MSV3drs63750572
GWAS Ctlgrs63750572
Max Magnitude0
ClinVar
Risk rs63750572(;)
Alt rs63750572(;)
Reference rs63750572(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703704delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076421.2,