Have questions? Visit https://www.reddit.com/r/SNPedia

rs63751206

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCTA;CCTA) 0 common in clinvar
(CTAC;CTAC) 0 common in clinvar
Make rs63751206(-;-)
Make rs63751206(-;CCTA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429908
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751206
ebirs63751206
HLIrs63751206
Exacrs63751206
Varsomers63751206
Maprs63751206
PheGenIrs63751206
hapmaprs63751206
1000 genomesrs63751206
hgdprs63751206
ensemblrs63751206
gopubmedrs63751206
geneviewrs63751206
scholarrs63751206
googlers63751206
pharmgkbrs63751206
gwascentralrs63751206
openSNPrs63751206
23andMers63751206
23andMe allrs63751206
SNP Nexus

SNPshotrs63751206
SNPdbers63751206
MSV3drs63751206
GWAS Ctlgrs63751206
Max Magnitude0
ClinVar
Risk rs63751206(;)
Alt rs63751206(;)
Reference rs63751206(CTAC;CTAC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47657047_47657050delCCTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076076.2,