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rs587783056

From SNPedia

Orientationplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs587783056(-;-)
Make rs587783056(-;TT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799688
GeneMSH6
is asnp
is mentioned by
dbSNPrs587783056
ebirs587783056
HLIrs587783056
Exacrs587783056
Varsomers587783056
Maprs587783056
PheGenIrs587783056
hapmaprs587783056
1000 genomesrs587783056
hgdprs587783056
ensemblrs587783056
gopubmedrs587783056
geneviewrs587783056
scholarrs587783056
googlers587783056
pharmgkbrs587783056
gwascentralrs587783056
openSNPrs587783056
23andMers587783056
23andMe allrs587783056
SNP Nexus

SNPshotrs587783056
SNPdbers587783056
MSV3drs587783056
GWAS Ctlgrs587783056
Max Magnitude0
ClinVar
Risk rs587783056(;)
Alt rs587783056(;)
Reference rs587783056(TT;TT)
Significance Pathogenic
Disease Lynch syndrome I Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH6
CLNDBN Lynch syndrome I Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48026827_48026828delTT
CLNSRC
CLNACC RCV000144627.1, RCV000216742.1,