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rs63751412

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751412(C;T)
Make rs63751412(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429869
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751412
ebirs63751412
HLIrs63751412
Exacrs63751412
Varsomers63751412
Maprs63751412
PheGenIrs63751412
hapmaprs63751412
1000 genomesrs63751412
hgdprs63751412
ensemblrs63751412
gopubmedrs63751412
geneviewrs63751412
scholarrs63751412
googlers63751412
pharmgkbrs63751412
gwascentralrs63751412
openSNPrs63751412
23andMers63751412
23andMe allrs63751412
SNP Nexus

SNPshotrs63751412
SNPdbers63751412
MSV3drs63751412
GWAS Ctlgrs63751412
Max Magnitude0
ClinVar
Risk rs63751412(A,T;A,T)
Alt rs63751412(A,T;A,T)
Reference rs63751412(C;C)
Significance Pathogenic
Disease not specified Lynch syndrome
Variation info
Gene MSH2
CLNDBN not specified Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47657008C>A; NC_000002.11:g.47657008C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000115497.3, RCV000206195.1, RCV000076061.2,