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rs63751444

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751444(G;G)
Make rs63751444(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410287
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751444
ebirs63751444
HLIrs63751444
Exacrs63751444
Varsomers63751444
Maprs63751444
PheGenIrs63751444
hapmaprs63751444
1000 genomesrs63751444
hgdprs63751444
ensemblrs63751444
gopubmedrs63751444
geneviewrs63751444
scholarrs63751444
googlers63751444
pharmgkbrs63751444
gwascentralrs63751444
openSNPrs63751444
23andMers63751444
23andMe allrs63751444
SNP Nexus

SNPshotrs63751444
SNPdbers63751444
MSV3drs63751444
GWAS Ctlgrs63751444
Max Magnitude0
ClinVar
Risk rs63751444(C,G;C,G)
Alt rs63751444(C,G;C,G)
Reference rs63751444(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637426T>C; NC_000002.11:g.47637426T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076638.2, RCV000076639.2,