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rs63750104

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63750104(-;-)
Make rs63750104(-;G)
Make rs63750104(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47466741
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750104
ebirs63750104
HLIrs63750104
Exacrs63750104
Varsomers63750104
Maprs63750104
PheGenIrs63750104
hapmaprs63750104
1000 genomesrs63750104
hgdprs63750104
ensemblrs63750104
gopubmedrs63750104
geneviewrs63750104
scholarrs63750104
googlers63750104
pharmgkbrs63750104
gwascentralrs63750104
openSNPrs63750104
23andMers63750104
23andMe allrs63750104
SNP Nexus

SNPshotrs63750104
SNPdbers63750104
MSV3drs63750104
GWAS Ctlgrs63750104
Max Magnitude0
ClinVar
Risk rs63750104(G;G)
Alt rs63750104(G;G)
Reference rs63750104(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47693880dupG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076203.2,