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rs63750103

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750103(-;-)
Make rs63750103(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475025
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750103
ebirs63750103
HLIrs63750103
Exacrs63750103
Varsomers63750103
Maprs63750103
PheGenIrs63750103
hapmaprs63750103
1000 genomesrs63750103
hgdprs63750103
ensemblrs63750103
gopubmedrs63750103
geneviewrs63750103
scholarrs63750103
googlers63750103
pharmgkbrs63750103
gwascentralrs63750103
openSNPrs63750103
23andMers63750103
23andMe allrs63750103
SNP Nexus

SNPshotrs63750103
SNPdbers63750103
MSV3drs63750103
GWAS Ctlgrs63750103
Max Magnitude0
ClinVar
Risk rs63750103(;)
Alt rs63750103(;)
Reference rs63750103(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702164delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076278.2,