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rs63750893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750893(-;-)
Make rs63750893(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475176
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750893
ebirs63750893
HLIrs63750893
Exacrs63750893
Varsomers63750893
Maprs63750893
PheGenIrs63750893
hapmaprs63750893
1000 genomesrs63750893
hgdprs63750893
ensemblrs63750893
gopubmedrs63750893
geneviewrs63750893
scholarrs63750893
googlers63750893
pharmgkbrs63750893
gwascentralrs63750893
openSNPrs63750893
23andMers63750893
23andMe allrs63750893
SNP Nexus

SNPshotrs63750893
SNPdbers63750893
MSV3drs63750893
GWAS Ctlgrs63750893
Max Magnitude0
ClinVar
Risk rs63750893(;)
Alt rs63750893(;)
Reference rs63750893(C;C)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47702315delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076318.2, RCV000201962.1,