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rs63750346

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(I;I) 0
Make rs63750346(-;-)
Make rs63750346(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478355
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750346
ebirs63750346
HLIrs63750346
Exacrs63750346
Varsomers63750346
Maprs63750346
PheGenIrs63750346
hapmaprs63750346
1000 genomesrs63750346
hgdprs63750346
ensemblrs63750346
gopubmedrs63750346
geneviewrs63750346
scholarrs63750346
googlers63750346
pharmgkbrs63750346
gwascentralrs63750346
openSNPrs63750346
23andMers63750346
23andMe allrs63750346
SNP Nexus

SNPshotrs63750346
SNPdbers63750346
MSV3drs63750346
GWAS Ctlgrs63750346
Max Magnitude0
ClinVar
Risk rs63750346(;)
Alt rs63750346(;)
Reference rs63750346(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705494delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076453.2,