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rs63750091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63750091(-;-)
Make rs63750091(-;T)
Make rs63750091(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47414315
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750091
ebirs63750091
HLIrs63750091
Exacrs63750091
Varsomers63750091
Maprs63750091
PheGenIrs63750091
hapmaprs63750091
1000 genomesrs63750091
hgdprs63750091
ensemblrs63750091
gopubmedrs63750091
geneviewrs63750091
scholarrs63750091
googlers63750091
pharmgkbrs63750091
gwascentralrs63750091
openSNPrs63750091
23andMers63750091
23andMe allrs63750091
SNP Nexus

SNPshotrs63750091
SNPdbers63750091
MSV3drs63750091
GWAS Ctlgrs63750091
Max Magnitude0
ClinVar
Risk rs63750091(T;T)
Alt rs63750091(T;T)
Reference rs63750091(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641454dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076733.2,