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rs63751453

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63751453(-;-)
Make rs63751453(-;T)
Make rs63751453(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476496
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751453
ebirs63751453
HLIrs63751453
Exacrs63751453
Varsomers63751453
Maprs63751453
PheGenIrs63751453
hapmaprs63751453
1000 genomesrs63751453
hgdprs63751453
ensemblrs63751453
gopubmedrs63751453
geneviewrs63751453
scholarrs63751453
googlers63751453
pharmgkbrs63751453
gwascentralrs63751453
openSNPrs63751453
23andMers63751453
23andMe allrs63751453
SNP Nexus

SNPshotrs63751453
SNPdbers63751453
MSV3drs63751453
GWAS Ctlgrs63751453
Max Magnitude0
ClinVar
Risk rs63751453(T;T)
Alt rs63751453(T;T)
Reference rs63751453(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703635dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076406.2,