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rs63750808

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750808(C;T)
Make rs63750808(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47482797
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750808
ebirs63750808
HLIrs63750808
Exacrs63750808
Varsomers63750808
Maprs63750808
PheGenIrs63750808
hapmaprs63750808
1000 genomesrs63750808
hgdprs63750808
ensemblrs63750808
gopubmedrs63750808
geneviewrs63750808
scholarrs63750808
googlers63750808
pharmgkbrs63750808
gwascentralrs63750808
openSNPrs63750808
23andMers63750808
23andMe allrs63750808
SNP Nexus

SNPshotrs63750808
SNPdbers63750808
MSV3drs63750808
GWAS Ctlgrs63750808
Max Magnitude0
ClinVar
Risk rs63750808(T;T)
Alt rs63750808(T;T)
Reference rs63750808(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.47709936C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076535.2, RCV000202119.1,