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rs63751156

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATTC;ATTC) 0 common in clinvar
(CATT;CATT) 0 common in clinvar
Make rs63751156(-;-)
Make rs63751156(-;CATT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478289
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751156
ebirs63751156
HLIrs63751156
Exacrs63751156
Varsomers63751156
Maprs63751156
PheGenIrs63751156
hapmaprs63751156
1000 genomesrs63751156
hgdprs63751156
ensemblrs63751156
gopubmedrs63751156
geneviewrs63751156
scholarrs63751156
googlers63751156
pharmgkbrs63751156
gwascentralrs63751156
openSNPrs63751156
23andMers63751156
23andMe allrs63751156
SNP Nexus

SNPshotrs63751156
SNPdbers63751156
MSV3drs63751156
GWAS Ctlgrs63751156
Max Magnitude0
ClinVar
Risk rs63751156(;)
Alt rs63751156(;)
Reference rs63751156(ATTC;ATTC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705428_47705431delCATT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076436.2,