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rs63750633

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(T;T) 0 common in clinvar
Make rs63750633(-;-)
Make rs63750633(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47470979
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750633
ebirs63750633
HLIrs63750633
Exacrs63750633
Varsomers63750633
Maprs63750633
PheGenIrs63750633
hapmaprs63750633
1000 genomesrs63750633
hgdprs63750633
ensemblrs63750633
gopubmedrs63750633
geneviewrs63750633
scholarrs63750633
googlers63750633
pharmgkbrs63750633
gwascentralrs63750633
openSNPrs63750633
23andMers63750633
23andMe allrs63750633
SNP Nexus

SNPshotrs63750633
SNPdbers63750633
MSV3drs63750633
GWAS Ctlgrs63750633
Max Magnitude0
ClinVar
Risk rs63750633(;)
Alt rs63750633(;)
Reference rs63750633(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698118delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076240.2,