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rs63750199

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750199(-;-)
Make rs63750199(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47403395
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750199
ebirs63750199
HLIrs63750199
Exacrs63750199
Varsomers63750199
Maprs63750199
PheGenIrs63750199
hapmaprs63750199
1000 genomesrs63750199
hgdprs63750199
ensemblrs63750199
gopubmedrs63750199
geneviewrs63750199
scholarrs63750199
googlers63750199
pharmgkbrs63750199
gwascentralrs63750199
openSNPrs63750199
23andMers63750199
23andMe allrs63750199
SNP Nexus

SNPshotrs63750199
SNPdbers63750199
MSV3drs63750199
GWAS Ctlgrs63750199
Max Magnitude0
ClinVar
Risk rs63750199(;)
Alt rs63750199(;)
Reference rs63750199(G;G)
Significance Pathogenic
Disease Lynch syndrome Lynch syndrome I
Variation info
Gene MSH2
CLNDBN Lynch syndrome Lynch syndrome I
Reversed 0
HGVS NC_000002.11:g.47630534delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076373.2, RCV000168722.1,