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rs63751195

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63751195(-;-)
Make rs63751195(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47408533
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751195
ebirs63751195
HLIrs63751195
Exacrs63751195
Varsomers63751195
Maprs63751195
PheGenIrs63751195
hapmaprs63751195
1000 genomesrs63751195
hgdprs63751195
ensemblrs63751195
gopubmedrs63751195
geneviewrs63751195
scholarrs63751195
googlers63751195
pharmgkbrs63751195
gwascentralrs63751195
openSNPrs63751195
23andMers63751195
23andMe allrs63751195
SNP Nexus

SNPshotrs63751195
SNPdbers63751195
MSV3drs63751195
GWAS Ctlgrs63751195
Max Magnitude0
ClinVar
Risk rs63751195(;)
Alt rs63751195(;)
Reference rs63751195(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47635672delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076568.2,