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rs63751328

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751328(A;A)
Make rs63751328(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47805638
GeneMSH6
is asnp
is mentioned by
dbSNPrs63751328
ebirs63751328
HLIrs63751328
Exacrs63751328
Varsomers63751328
Maprs63751328
PheGenIrs63751328
hapmaprs63751328
1000 genomesrs63751328
hgdprs63751328
ensemblrs63751328
gopubmedrs63751328
geneviewrs63751328
scholarrs63751328
googlers63751328
pharmgkbrs63751328
gwascentralrs63751328
openSNPrs63751328
23andMers63751328
23andMe allrs63751328
SNP Nexus

SNPshotrs63751328
SNPdbers63751328
MSV3drs63751328
GWAS Ctlgrs63751328
Max Magnitude0
ClinVar
Risk rs63751328(A;A)
Alt rs63751328(A;A)
Reference rs63751328(G;G)
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.48032777G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074890.2, RCV000166108.1,