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rs63750439

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
(TA;TA) 0 common in clinvar
Make rs63750439(-;-)
Make rs63750439(-;AT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47799173
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750439
ebirs63750439
HLIrs63750439
Exacrs63750439
Varsomers63750439
Maprs63750439
PheGenIrs63750439
hapmaprs63750439
1000 genomesrs63750439
hgdprs63750439
ensemblrs63750439
gopubmedrs63750439
geneviewrs63750439
scholarrs63750439
googlers63750439
pharmgkbrs63750439
gwascentralrs63750439
openSNPrs63750439
23andMers63750439
23andMe allrs63750439
SNP Nexus

SNPshotrs63750439
SNPdbers63750439
MSV3drs63750439
GWAS Ctlgrs63750439
Max Magnitude0
ClinVar
Risk rs63750439(;)
Alt rs63750439(;)
Reference rs63750439(TA;TA)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48026312_48026313delAT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074640.2, RCV000160740.1,