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rs63750737

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs63750737(-;-)
Make rs63750737(-;AA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47470999
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750737
ebirs63750737
HLIrs63750737
Exacrs63750737
Varsomers63750737
Maprs63750737
PheGenIrs63750737
hapmaprs63750737
1000 genomesrs63750737
hgdprs63750737
ensemblrs63750737
gopubmedrs63750737
geneviewrs63750737
scholarrs63750737
googlers63750737
pharmgkbrs63750737
gwascentralrs63750737
openSNPrs63750737
23andMers63750737
23andMe allrs63750737
SNP Nexus

SNPshotrs63750737
SNPdbers63750737
MSV3drs63750737
GWAS Ctlgrs63750737
Max Magnitude0
ClinVar
Risk rs63750737(;)
Alt rs63750737(;)
Reference rs63750737(AA;AA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698138_47698139delAA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076249.2,