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rs63750296

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750296(-;-)
Make rs63750296(-;A)
Make rs63750296(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47804990
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750296
ebirs63750296
HLIrs63750296
Exacrs63750296
Varsomers63750296
Maprs63750296
PheGenIrs63750296
hapmaprs63750296
1000 genomesrs63750296
hgdprs63750296
ensemblrs63750296
gopubmedrs63750296
geneviewrs63750296
scholarrs63750296
googlers63750296
pharmgkbrs63750296
gwascentralrs63750296
openSNPrs63750296
23andMers63750296
23andMe allrs63750296
SNP Nexus

SNPshotrs63750296
SNPdbers63750296
MSV3drs63750296
GWAS Ctlgrs63750296
Max Magnitude0
ClinVar
Risk rs63750296(A;A)
Alt rs63750296(A;A)
Reference rs63750296(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48032129_48032130insA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074875.2,