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rs63750984

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750984(-;-)
Make rs63750984(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47403310
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750984
ebirs63750984
HLIrs63750984
Exacrs63750984
Varsomers63750984
Maprs63750984
PheGenIrs63750984
hapmaprs63750984
1000 genomesrs63750984
hgdprs63750984
ensemblrs63750984
gopubmedrs63750984
geneviewrs63750984
scholarrs63750984
googlers63750984
pharmgkbrs63750984
gwascentralrs63750984
openSNPrs63750984
23andMers63750984
23andMe allrs63750984
SNP Nexus

SNPshotrs63750984
SNPdbers63750984
MSV3drs63750984
GWAS Ctlgrs63750984
Max Magnitude0
ClinVar
Risk rs63750984(;)
Alt rs63750984(;)
Reference rs63750984(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630449delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076059.2,