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rs63751120

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63751120(-;-)
Make rs63751120(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47470968
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751120
ebirs63751120
HLIrs63751120
Exacrs63751120
Varsomers63751120
Maprs63751120
PheGenIrs63751120
hapmaprs63751120
1000 genomesrs63751120
hgdprs63751120
ensemblrs63751120
gopubmedrs63751120
geneviewrs63751120
scholarrs63751120
googlers63751120
pharmgkbrs63751120
gwascentralrs63751120
openSNPrs63751120
23andMers63751120
23andMe allrs63751120
SNP Nexus

SNPshotrs63751120
SNPdbers63751120
MSV3drs63751120
GWAS Ctlgrs63751120
Max Magnitude0
ClinVar
Risk rs63751120(;)
Alt rs63751120(;)
Reference rs63751120(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698107delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076233.2,