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rs63750957

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs63750957(-;-)
Make rs63750957(-;AG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47445623
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750957
ebirs63750957
HLIrs63750957
Exacrs63750957
Varsomers63750957
Maprs63750957
PheGenIrs63750957
hapmaprs63750957
1000 genomesrs63750957
hgdprs63750957
ensemblrs63750957
gopubmedrs63750957
geneviewrs63750957
scholarrs63750957
googlers63750957
pharmgkbrs63750957
gwascentralrs63750957
openSNPrs63750957
23andMers63750957
23andMe allrs63750957
SNP Nexus

SNPshotrs63750957
SNPdbers63750957
MSV3drs63750957
GWAS Ctlgrs63750957
Max Magnitude0
ClinVar
Risk rs63750957(;)
Alt rs63750957(;)
Reference rs63750957(AG;AG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47672762_47672763delAG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076131.2,