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rs63750352

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750352(-;-)
Make rs63750352(-;G)
Make rs63750352(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47403345
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750352
ebirs63750352
HLIrs63750352
Exacrs63750352
Varsomers63750352
Maprs63750352
PheGenIrs63750352
hapmaprs63750352
1000 genomesrs63750352
hgdprs63750352
ensemblrs63750352
gopubmedrs63750352
geneviewrs63750352
scholarrs63750352
googlers63750352
pharmgkbrs63750352
gwascentralrs63750352
openSNPrs63750352
23andMers63750352
23andMe allrs63750352
SNP Nexus

SNPshotrs63750352
SNPdbers63750352
MSV3drs63750352
GWAS Ctlgrs63750352
Max Magnitude0
ClinVar
Risk rs63750352(G;G)
Alt rs63750352(G;G)
Reference rs63750352(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630484_47630485insG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076191.2,