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rs63751158

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63751158(-;-)
Make rs63751158(-;T)
Make rs63751158(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47408444
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751158
ebirs63751158
HLIrs63751158
Exacrs63751158
Varsomers63751158
Maprs63751158
PheGenIrs63751158
hapmaprs63751158
1000 genomesrs63751158
hgdprs63751158
ensemblrs63751158
gopubmedrs63751158
geneviewrs63751158
scholarrs63751158
googlers63751158
pharmgkbrs63751158
gwascentralrs63751158
openSNPrs63751158
23andMers63751158
23andMe allrs63751158
SNP Nexus

SNPshotrs63751158
SNPdbers63751158
MSV3drs63751158
GWAS Ctlgrs63751158
Max Magnitude0
ClinVar
Risk rs63751158(T;T)
Alt rs63751158(T;T)
Reference rs63751158(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47635583dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076504.2,