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rs63749945

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63749945(-;-)
Make rs63749945(-;T)
Make rs63749945(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47416326
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749945
ebirs63749945
HLIrs63749945
Exacrs63749945
Varsomers63749945
Maprs63749945
PheGenIrs63749945
hapmaprs63749945
1000 genomesrs63749945
hgdprs63749945
ensemblrs63749945
gopubmedrs63749945
geneviewrs63749945
scholarrs63749945
googlers63749945
pharmgkbrs63749945
gwascentralrs63749945
openSNPrs63749945
23andMers63749945
23andMe allrs63749945
SNP Nexus

SNPshotrs63749945
SNPdbers63749945
MSV3drs63749945
GWAS Ctlgrs63749945
Max Magnitude0
ClinVar
Risk rs63749945(T;T)
Alt rs63749945(T;T)
Reference rs63749945(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47643465dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076771.2,