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rs63751626

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63751626(-;-)
Make rs63751626(-;G)
Make rs63751626(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47445558
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751626
ebirs63751626
HLIrs63751626
Exacrs63751626
Varsomers63751626
Maprs63751626
PheGenIrs63751626
hapmaprs63751626
1000 genomesrs63751626
hgdprs63751626
ensemblrs63751626
gopubmedrs63751626
geneviewrs63751626
scholarrs63751626
googlers63751626
pharmgkbrs63751626
gwascentralrs63751626
openSNPrs63751626
23andMers63751626
23andMe allrs63751626
SNP Nexus

SNPshotrs63751626
SNPdbers63751626
MSV3drs63751626
GWAS Ctlgrs63751626
Max Magnitude0
ClinVar
Risk rs63751626(G;G)
Alt rs63751626(G;G)
Reference rs63751626(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47672697dupG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076113.2,