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rs63750426

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs63750426(-;-)
Make rs63750426(-;TT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47412464
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750426
ebirs63750426
HLIrs63750426
Exacrs63750426
Varsomers63750426
Maprs63750426
PheGenIrs63750426
hapmaprs63750426
1000 genomesrs63750426
hgdprs63750426
ensemblrs63750426
gopubmedrs63750426
geneviewrs63750426
scholarrs63750426
googlers63750426
pharmgkbrs63750426
gwascentralrs63750426
openSNPrs63750426
23andMers63750426
23andMe allrs63750426
SNP Nexus

SNPshotrs63750426
SNPdbers63750426
MSV3drs63750426
GWAS Ctlgrs63750426
Max Magnitude0
ClinVar
Risk rs63750426(;)
Alt rs63750426(;)
Reference rs63750426(TT;TT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639603_47639604delTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076684.2,