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rs63750087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(I;I) 0
Make rs63750087(-;-)
Make rs63750087(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47403357
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750087
ebirs63750087
HLIrs63750087
Exacrs63750087
Varsomers63750087
Maprs63750087
PheGenIrs63750087
hapmaprs63750087
1000 genomesrs63750087
hgdprs63750087
ensemblrs63750087
gopubmedrs63750087
geneviewrs63750087
scholarrs63750087
googlers63750087
pharmgkbrs63750087
gwascentralrs63750087
openSNPrs63750087
23andMers63750087
23andMe allrs63750087
SNP Nexus

SNPshotrs63750087
SNPdbers63750087
MSV3drs63750087
GWAS Ctlgrs63750087
Max Magnitude0
ClinVar
Risk rs63750087(;)
Alt rs63750087(;)
Reference rs63750087(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630496delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076239.2,