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rs63750586

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750586(-;-)
Make rs63750586(-;A)
Make rs63750586(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429868
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750586
ebirs63750586
HLIrs63750586
Exacrs63750586
Varsomers63750586
Maprs63750586
PheGenIrs63750586
hapmaprs63750586
1000 genomesrs63750586
hgdprs63750586
ensemblrs63750586
gopubmedrs63750586
geneviewrs63750586
scholarrs63750586
googlers63750586
pharmgkbrs63750586
gwascentralrs63750586
openSNPrs63750586
23andMers63750586
23andMe allrs63750586
SNP Nexus

SNPshotrs63750586
SNPdbers63750586
MSV3drs63750586
GWAS Ctlgrs63750586
Max Magnitude0
ClinVar
Risk rs63750586(A;A)
Alt rs63750586(A;A)
Reference rs63750586(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47657007dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076060.2,