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rs63750337

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750337(-;-)
Make rs63750337(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47403354
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750337
ebirs63750337
HLIrs63750337
Exacrs63750337
Varsomers63750337
Maprs63750337
PheGenIrs63750337
hapmaprs63750337
1000 genomesrs63750337
hgdprs63750337
ensemblrs63750337
gopubmedrs63750337
geneviewrs63750337
scholarrs63750337
googlers63750337
pharmgkbrs63750337
gwascentralrs63750337
openSNPrs63750337
23andMers63750337
23andMe allrs63750337
SNP Nexus

SNPshotrs63750337
SNPdbers63750337
MSV3drs63750337
GWAS Ctlgrs63750337
Max Magnitude0
ClinVar
Risk rs63750337(;)
Alt rs63750337(;)
Reference rs63750337(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630493delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076209.2,