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rs63750854

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750854(-;-)
Make rs63750854(-;TG)
Make rs63750854(TG;TG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47799405
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750854
ebirs63750854
HLIrs63750854
Exacrs63750854
Varsomers63750854
Maprs63750854
PheGenIrs63750854
hapmaprs63750854
1000 genomesrs63750854
hgdprs63750854
ensemblrs63750854
gopubmedrs63750854
geneviewrs63750854
scholarrs63750854
googlers63750854
pharmgkbrs63750854
gwascentralrs63750854
openSNPrs63750854
23andMers63750854
23andMe allrs63750854
SNP Nexus

SNPshotrs63750854
SNPdbers63750854
MSV3drs63750854
GWAS Ctlgrs63750854
Max Magnitude0
ClinVar
Risk rs63750854(GT;GT)
Alt rs63750854(GT;GT)
Reference rs63750854(;)
Significance Pathogenic
Disease Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH6
CLNDBN Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48026543_48026544dupTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074655.2, RCV000222326.1,