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rs63751602

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AATTC;AATTC) 0 common in clinvar
(TTCAA;TTCAA) 0 common in clinvar
Make rs63751602(-;-)
Make rs63751602(-;TTCAA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47412418
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751602
ebirs63751602
HLIrs63751602
Exacrs63751602
Varsomers63751602
Maprs63751602
PheGenIrs63751602
hapmaprs63751602
1000 genomesrs63751602
hgdprs63751602
ensemblrs63751602
gopubmedrs63751602
geneviewrs63751602
scholarrs63751602
googlers63751602
pharmgkbrs63751602
gwascentralrs63751602
openSNPrs63751602
23andMers63751602
23andMe allrs63751602
SNP Nexus

SNPshotrs63751602
SNPdbers63751602
MSV3drs63751602
GWAS Ctlgrs63751602
Max Magnitude0
ClinVar
Risk rs63751602(;)
Alt rs63751602(;)
Reference rs63751602(AATTC;AATTC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639557_47639561delTTCAA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076676.2,