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rs63750806

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63750806(-;-)
Make rs63750806(-;GT)
Make rs63750806(GT;GT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475124
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750806
ebirs63750806
HLIrs63750806
Exacrs63750806
Varsomers63750806
Maprs63750806
PheGenIrs63750806
hapmaprs63750806
1000 genomesrs63750806
hgdprs63750806
ensemblrs63750806
gopubmedrs63750806
geneviewrs63750806
scholarrs63750806
googlers63750806
pharmgkbrs63750806
gwascentralrs63750806
openSNPrs63750806
23andMers63750806
23andMe allrs63750806
SNP Nexus

SNPshotrs63750806
SNPdbers63750806
MSV3drs63750806
GWAS Ctlgrs63750806
Max Magnitude0
ClinVar
Risk rs63750806(TG;TG)
Alt rs63750806(TG;TG)
Reference rs63750806(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702262_47702263dupGT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076304.2,