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rs63750086

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(I;I) 0
Make rs63750086(-;-)
Make rs63750086(-;AG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429891
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750086
ebirs63750086
HLIrs63750086
Exacrs63750086
Varsomers63750086
Maprs63750086
PheGenIrs63750086
hapmaprs63750086
1000 genomesrs63750086
hgdprs63750086
ensemblrs63750086
gopubmedrs63750086
geneviewrs63750086
scholarrs63750086
googlers63750086
pharmgkbrs63750086
gwascentralrs63750086
openSNPrs63750086
23andMers63750086
23andMe allrs63750086
SNP Nexus

SNPshotrs63750086
SNPdbers63750086
MSV3drs63750086
GWAS Ctlgrs63750086
Max Magnitude0
ClinVar
Risk rs63750086(;)
Alt rs63750086(;)
Reference rs63750086(AG;AG)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47657030_47657031delAG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076073.2, RCV000160629.3, RCV000212600.1,