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rs63750675

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(I;I) 0
Make rs63750675(-;-)
Make rs63750675(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47466774
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750675
ebirs63750675
HLIrs63750675
Exacrs63750675
Varsomers63750675
Maprs63750675
PheGenIrs63750675
hapmaprs63750675
1000 genomesrs63750675
hgdprs63750675
ensemblrs63750675
gopubmedrs63750675
geneviewrs63750675
scholarrs63750675
googlers63750675
pharmgkbrs63750675
gwascentralrs63750675
openSNPrs63750675
23andMers63750675
23andMe allrs63750675
SNP Nexus

SNPshotrs63750675
SNPdbers63750675
MSV3drs63750675
GWAS Ctlgrs63750675
Max Magnitude0
ClinVar
Risk rs63750675(;)
Alt rs63750675(;)
Reference rs63750675(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47693913delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076207.2,