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rs63751143

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(T;T) 0 common in clinvar
Make rs63751143(-;-)
Make rs63751143(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478356
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751143
ebirs63751143
HLIrs63751143
Exacrs63751143
Varsomers63751143
Maprs63751143
PheGenIrs63751143
hapmaprs63751143
1000 genomesrs63751143
hgdprs63751143
ensemblrs63751143
gopubmedrs63751143
geneviewrs63751143
scholarrs63751143
googlers63751143
pharmgkbrs63751143
gwascentralrs63751143
openSNPrs63751143
23andMers63751143
23andMe allrs63751143
SNP Nexus

SNPshotrs63751143
SNPdbers63751143
MSV3drs63751143
GWAS Ctlgrs63751143
Max Magnitude0
ClinVar
Risk rs63751143(;)
Alt rs63751143(;)
Reference rs63751143(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705495delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076454.2,