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rs63750738

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(I;I) 0
Make rs63750738(-;-)
Make rs63750738(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47466725
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750738
ebirs63750738
HLIrs63750738
Exacrs63750738
Varsomers63750738
Maprs63750738
PheGenIrs63750738
hapmaprs63750738
1000 genomesrs63750738
hgdprs63750738
ensemblrs63750738
gopubmedrs63750738
geneviewrs63750738
scholarrs63750738
googlers63750738
pharmgkbrs63750738
gwascentralrs63750738
openSNPrs63750738
23andMers63750738
23andMe allrs63750738
SNP Nexus

SNPshotrs63750738
SNPdbers63750738
MSV3drs63750738
GWAS Ctlgrs63750738
Max Magnitude0
ClinVar
Risk rs63750738(;)
Alt rs63750738(;)
Reference rs63750738(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47693864delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076200.2,