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rs63751695

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACAG;ACAG) 0 common in clinvar
(AGAC;AGAC) 0 common in clinvar
Make rs63751695(-;-)
Make rs63751695(-;ACAG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410369
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751695
ebirs63751695
HLIrs63751695
Exacrs63751695
Varsomers63751695
Maprs63751695
PheGenIrs63751695
hapmaprs63751695
1000 genomesrs63751695
hgdprs63751695
ensemblrs63751695
gopubmedrs63751695
geneviewrs63751695
scholarrs63751695
googlers63751695
pharmgkbrs63751695
gwascentralrs63751695
openSNPrs63751695
23andMers63751695
23andMe allrs63751695
SNP Nexus

SNPshotrs63751695
SNPdbers63751695
MSV3drs63751695
GWAS Ctlgrs63751695
Max Magnitude0
ClinVar
Risk rs63751695(;)
Alt rs63751695(;)
Reference rs63751695(AGAC;AGAC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637508_47637511delACAG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076657.2,