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rs63751604

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63751604(G;T)
Make rs63751604(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position47416429
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751604
ebirs63751604
HLIrs63751604
Exacrs63751604
Varsomers63751604
Maprs63751604
PheGenIrs63751604
hapmaprs63751604
1000 genomesrs63751604
hgdprs63751604
ensemblrs63751604
gopubmedrs63751604
geneviewrs63751604
scholarrs63751604
googlers63751604
pharmgkbrs63751604
gwascentralrs63751604
openSNPrs63751604
23andMers63751604
23andMe allrs63751604
SNP Nexus

SNPshotrs63751604
SNPdbers63751604
MSV3drs63751604
GWAS Ctlgrs63751604
Max Magnitude0
ClinVar
Risk rs63751604(A,C,T;A,C,T)
Alt rs63751604(A,C,T;A,C,T)
Reference rs63751604(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47643568G>C
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000132158.2, RCV000225952.1,