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rs63750701

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs63750701(-;-)
Make rs63750701(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47414330
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750701
ebirs63750701
HLIrs63750701
Exacrs63750701
Varsomers63750701
Maprs63750701
PheGenIrs63750701
hapmaprs63750701
1000 genomesrs63750701
hgdprs63750701
ensemblrs63750701
gopubmedrs63750701
geneviewrs63750701
scholarrs63750701
googlers63750701
pharmgkbrs63750701
gwascentralrs63750701
openSNPrs63750701
23andMers63750701
23andMe allrs63750701
SNP Nexus

SNPshotrs63750701
SNPdbers63750701
MSV3drs63750701
GWAS Ctlgrs63750701
Max Magnitude0
ClinVar
Risk rs63750701(;)
Alt rs63750701(;)
Reference rs63750701(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641469delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076736.2,