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rs63750119

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750119(G;T)
Make rs63750119(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position47806282
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750119
ebirs63750119
HLIrs63750119
Exacrs63750119
Varsomers63750119
Maprs63750119
PheGenIrs63750119
hapmaprs63750119
1000 genomesrs63750119
hgdprs63750119
ensemblrs63750119
gopubmedrs63750119
geneviewrs63750119
scholarrs63750119
googlers63750119
pharmgkbrs63750119
gwascentralrs63750119
openSNPrs63750119
23andMers63750119
23andMe allrs63750119
SNP Nexus

SNPshotrs63750119
SNPdbers63750119
MSV3drs63750119
GWAS Ctlgrs63750119
Max Magnitude0
ClinVar
Risk rs63750119(A,T;A,T)
Alt rs63750119(A,T;A,T)
Reference rs63750119(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033421G>A; NC_000002.11:g.48033421G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000129081.2, RCV000230170.1, RCV000074919.2, RCV000130075.2,