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rs63751113

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751113(A;A)
Make rs63751113(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47800910
GeneMSH6
is asnp
is mentioned by
dbSNPrs63751113
ebirs63751113
HLIrs63751113
Exacrs63751113
Varsomers63751113
Maprs63751113
PheGenIrs63751113
hapmaprs63751113
1000 genomesrs63751113
hgdprs63751113
ensemblrs63751113
gopubmedrs63751113
geneviewrs63751113
scholarrs63751113
googlers63751113
pharmgkbrs63751113
gwascentralrs63751113
openSNPrs63751113
23andMers63751113
23andMe allrs63751113
SNP Nexus

SNPshotrs63751113
SNPdbers63751113
MSV3drs63751113
GWAS Ctlgrs63751113
Max Magnitude0
ClinVar
Risk rs63751113(A;A)
Alt rs63751113(A;A)
Reference rs63751113(G;G)
Significance Probable-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.48028049G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074787.2, RCV000218618.1,