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rs63750408

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(T;T) 0 common in clinvar
Make rs63750408(-;-)
Make rs63750408(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410135
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750408
ebirs63750408
HLIrs63750408
Exacrs63750408
Varsomers63750408
Maprs63750408
PheGenIrs63750408
hapmaprs63750408
1000 genomesrs63750408
hgdprs63750408
ensemblrs63750408
gopubmedrs63750408
geneviewrs63750408
scholarrs63750408
googlers63750408
pharmgkbrs63750408
gwascentralrs63750408
openSNPrs63750408
23andMers63750408
23andMe allrs63750408
SNP Nexus

SNPshotrs63750408
SNPdbers63750408
MSV3drs63750408
GWAS Ctlgrs63750408
Max Magnitude0
ClinVar
Risk rs63750408(;)
Alt rs63750408(;)
Reference rs63750408(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637274delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076596.2,