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rs63750406

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750406(-;-)
Make rs63750406(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47470986
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750406
ebirs63750406
HLIrs63750406
Exacrs63750406
Varsomers63750406
Maprs63750406
PheGenIrs63750406
hapmaprs63750406
1000 genomesrs63750406
hgdprs63750406
ensemblrs63750406
gopubmedrs63750406
geneviewrs63750406
scholarrs63750406
googlers63750406
pharmgkbrs63750406
gwascentralrs63750406
openSNPrs63750406
23andMers63750406
23andMe allrs63750406
SNP Nexus

SNPshotrs63750406
SNPdbers63750406
MSV3drs63750406
GWAS Ctlgrs63750406
Max Magnitude0
ClinVar
Risk rs63750406(;)
Alt rs63750406(;)
Reference rs63750406(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698125delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076243.2,