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rs63750885

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63750885(-;-)
Make rs63750885(-;AT)
Make rs63750885(AT;AT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47414375
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750885
ebirs63750885
HLIrs63750885
Exacrs63750885
Varsomers63750885
Maprs63750885
PheGenIrs63750885
hapmaprs63750885
1000 genomesrs63750885
hgdprs63750885
ensemblrs63750885
gopubmedrs63750885
geneviewrs63750885
scholarrs63750885
googlers63750885
pharmgkbrs63750885
gwascentralrs63750885
openSNPrs63750885
23andMers63750885
23andMe allrs63750885
SNP Nexus

SNPshotrs63750885
SNPdbers63750885
MSV3drs63750885
GWAS Ctlgrs63750885
Max Magnitude0
ClinVar
Risk rs63750885(TA;TA)
Alt rs63750885(TA;TA)
Reference rs63750885(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641513_47641514dupAT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076745.2,