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rs63751099

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751099(C;T)
Make rs63751099(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47403219
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751099
ebirs63751099
HLIrs63751099
Exacrs63751099
Varsomers63751099
Maprs63751099
PheGenIrs63751099
hapmaprs63751099
1000 genomesrs63751099
hgdprs63751099
ensemblrs63751099
gopubmedrs63751099
geneviewrs63751099
scholarrs63751099
googlers63751099
pharmgkbrs63751099
gwascentralrs63751099
openSNPrs63751099
23andMers63751099
23andMe allrs63751099
SNP Nexus

SNPshotrs63751099
SNPdbers63751099
MSV3drs63751099
GWAS Ctlgrs63751099
Max Magnitude0
ClinVar
Risk rs63751099(A,T;A,T)
Alt rs63751099(A,T;A,T)
Reference rs63751099(C;C)
Significance Pathogenic
Disease not provided Lynch syndrome
Variation info
Gene MSH2
CLNDBN not provided Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630358C>A; NC_000002.11:g.47630358C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000034557.1, RCV000076557.2,