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rs63751013

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CATA;CATA) 0 common in clinvar
(TACA;TACA) 0 common in clinvar
Make rs63751013(-;-)
Make rs63751013(-;TACA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410233
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751013
ebirs63751013
HLIrs63751013
Exacrs63751013
Varsomers63751013
Maprs63751013
PheGenIrs63751013
hapmaprs63751013
1000 genomesrs63751013
hgdprs63751013
ensemblrs63751013
gopubmedrs63751013
geneviewrs63751013
scholarrs63751013
googlers63751013
pharmgkbrs63751013
gwascentralrs63751013
openSNPrs63751013
23andMers63751013
23andMe allrs63751013
SNP Nexus

SNPshotrs63751013
SNPdbers63751013
MSV3drs63751013
GWAS Ctlgrs63751013
Max Magnitude0
ClinVar
Risk rs63751013(;)
Alt rs63751013(;)
Reference rs63751013(CATA;CATA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637372_47637375delTACA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076620.2,