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rs63750384

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750384(-;-)
Make rs63750384(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47463052
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750384
ebirs63750384
HLIrs63750384
Exacrs63750384
Varsomers63750384
Maprs63750384
PheGenIrs63750384
hapmaprs63750384
1000 genomesrs63750384
hgdprs63750384
ensemblrs63750384
gopubmedrs63750384
geneviewrs63750384
scholarrs63750384
googlers63750384
pharmgkbrs63750384
gwascentralrs63750384
openSNPrs63750384
23andMers63750384
23andMe allrs63750384
SNP Nexus

SNPshotrs63750384
SNPdbers63750384
MSV3drs63750384
GWAS Ctlgrs63750384
Max Magnitude0
ClinVar
Risk rs63750384(;)
Alt rs63750384(;)
Reference rs63750384(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690191delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076153.2,