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rs63751288

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATTT;ATTT) 0 common in clinvar
(TTAT;TTAT) 0 common in clinvar
Make rs63751288(-;-)
Make rs63751288(-;TTAT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47412479
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751288
ebirs63751288
HLIrs63751288
Exacrs63751288
Varsomers63751288
Maprs63751288
PheGenIrs63751288
hapmaprs63751288
1000 genomesrs63751288
hgdprs63751288
ensemblrs63751288
gopubmedrs63751288
geneviewrs63751288
scholarrs63751288
googlers63751288
pharmgkbrs63751288
gwascentralrs63751288
openSNPrs63751288
23andMers63751288
23andMe allrs63751288
SNP Nexus

SNPshotrs63751288
SNPdbers63751288
MSV3drs63751288
GWAS Ctlgrs63751288
Max Magnitude0
ClinVar
Risk rs63751288(;)
Alt rs63751288(;)
Reference rs63751288(ATTT;ATTT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639618_47639621delTTAT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076688.2,