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rs63751600

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751600(C;C)
Make rs63751600(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47463154
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751600
ebirs63751600
HLIrs63751600
Exacrs63751600
Varsomers63751600
Maprs63751600
PheGenIrs63751600
hapmaprs63751600
1000 genomesrs63751600
hgdprs63751600
ensemblrs63751600
gopubmedrs63751600
geneviewrs63751600
scholarrs63751600
googlers63751600
pharmgkbrs63751600
gwascentralrs63751600
openSNPrs63751600
23andMers63751600
23andMe allrs63751600
SNP Nexus

SNPshotrs63751600
SNPdbers63751600
MSV3drs63751600
GWAS Ctlgrs63751600
Max Magnitude0
ClinVar
Risk rs63751600(C,T;C,T)
Alt rs63751600(C,T;C,T)
Reference rs63751600(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690293G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076181.2,