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rs63750845

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs63750845(-;-)
Make rs63750845(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47466734
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750845
ebirs63750845
HLIrs63750845
Exacrs63750845
Varsomers63750845
Maprs63750845
PheGenIrs63750845
hapmaprs63750845
1000 genomesrs63750845
hgdprs63750845
ensemblrs63750845
gopubmedrs63750845
geneviewrs63750845
scholarrs63750845
googlers63750845
pharmgkbrs63750845
gwascentralrs63750845
openSNPrs63750845
23andMers63750845
23andMe allrs63750845
SNP Nexus

SNPshotrs63750845
SNPdbers63750845
MSV3drs63750845
GWAS Ctlgrs63750845
Max Magnitude0
ClinVar
Risk rs63750845(;)
Alt rs63750845(;)
Reference rs63750845(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47693873delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076201.2,