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rs63750094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs63750094(-;-)
Make rs63750094(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47466723
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750094
ebirs63750094
HLIrs63750094
Exacrs63750094
Varsomers63750094
Maprs63750094
PheGenIrs63750094
hapmaprs63750094
1000 genomesrs63750094
hgdprs63750094
ensemblrs63750094
gopubmedrs63750094
geneviewrs63750094
scholarrs63750094
googlers63750094
pharmgkbrs63750094
gwascentralrs63750094
openSNPrs63750094
23andMers63750094
23andMe allrs63750094
SNP Nexus

SNPshotrs63750094
SNPdbers63750094
MSV3drs63750094
GWAS Ctlgrs63750094
Max Magnitude0
ClinVar
Risk rs63750094(;)
Alt rs63750094(;)
Reference rs63750094(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47693862delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076199.2,