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rs63750474

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAAC;AAAAC) 0 common in clinvar
(AAACA;AAACA) 0 common in clinvar
Make rs63750474(-;-)
Make rs63750474(-;AAACA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47471003
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750474
ebirs63750474
HLIrs63750474
Exacrs63750474
Varsomers63750474
Maprs63750474
PheGenIrs63750474
hapmaprs63750474
1000 genomesrs63750474
hgdprs63750474
ensemblrs63750474
gopubmedrs63750474
geneviewrs63750474
scholarrs63750474
googlers63750474
pharmgkbrs63750474
gwascentralrs63750474
openSNPrs63750474
23andMers63750474
23andMe allrs63750474
SNP Nexus

SNPshotrs63750474
SNPdbers63750474
MSV3drs63750474
GWAS Ctlgrs63750474
Max Magnitude0
ClinVar
Risk rs63750474(;)
Alt rs63750474(;)
Reference rs63750474(AAAAC;AAAAC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698142_47698146delAAACA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076252.2,