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

rs63751656

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63751656(A;C)
Make rs63751656(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47466807
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751656
ebirs63751656
HLIrs63751656
Exacrs63751656
Varsomers63751656
Maprs63751656
PheGenIrs63751656
hapmaprs63751656
1000 genomesrs63751656
hgdprs63751656
ensemblrs63751656
gopubmedrs63751656
geneviewrs63751656
scholarrs63751656
googlers63751656
pharmgkbrs63751656
gwascentralrs63751656
openSNPrs63751656
23andMers63751656
23andMe allrs63751656
SNP Nexus

SNPshotrs63751656
SNPdbers63751656
MSV3drs63751656
GWAS Ctlgrs63751656
Max Magnitude0
ClinVar
Risk rs63751656(C,G,T;C,G,T)
Alt rs63751656(C,G,T;C,G,T)
Reference rs63751656(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47693946A>C; NC_000002.11:g.47693946A>G; NC_000002.11:g.47693946A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076213.2, RCV000076214.2, RCV000076215.2,