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rs63750617

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750617(C;T)
Make rs63750617(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47803473
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750617
ebirs63750617
HLIrs63750617
Exacrs63750617
Varsomers63750617
Maprs63750617
PheGenIrs63750617
hapmaprs63750617
1000 genomesrs63750617
hgdprs63750617
ensemblrs63750617
gopubmedrs63750617
geneviewrs63750617
scholarrs63750617
googlers63750617
pharmgkbrs63750617
gwascentralrs63750617
openSNPrs63750617
23andMers63750617
23andMe allrs63750617
SNP Nexus

SNPshotrs63750617
SNPdbers63750617
MSV3drs63750617
GWAS Ctlgrs63750617
Max Magnitude0
ClinVar
Risk rs63750617(G,T;G,T)
Alt rs63750617(G,T;G,T)
Reference rs63750617(C;C)
Significance Probable-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.48030612C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074823.2, RCV000162445.1,