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rs63750060

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs63750060(-;-)
Make rs63750060(-;CA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478469
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750060
ebirs63750060
HLIrs63750060
Exacrs63750060
Varsomers63750060
Maprs63750060
PheGenIrs63750060
hapmaprs63750060
1000 genomesrs63750060
hgdprs63750060
ensemblrs63750060
gopubmedrs63750060
geneviewrs63750060
scholarrs63750060
googlers63750060
pharmgkbrs63750060
gwascentralrs63750060
openSNPrs63750060
23andMers63750060
23andMe allrs63750060
SNP Nexus

SNPshotrs63750060
SNPdbers63750060
MSV3drs63750060
GWAS Ctlgrs63750060
Max Magnitude0
ClinVar
Risk rs63750060(;)
Alt rs63750060(;)
Reference rs63750060(CA;CA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705608_47705609delCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076468.2,