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rs63750161

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(GA;GA) 0 common in clinvar
Make rs63750161(-;-)
Make rs63750161(-;GA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47463091
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750161
ebirs63750161
HLIrs63750161
Exacrs63750161
Varsomers63750161
Maprs63750161
PheGenIrs63750161
hapmaprs63750161
1000 genomesrs63750161
hgdprs63750161
ensemblrs63750161
gopubmedrs63750161
geneviewrs63750161
scholarrs63750161
googlers63750161
pharmgkbrs63750161
gwascentralrs63750161
openSNPrs63750161
23andMers63750161
23andMe allrs63750161
SNP Nexus

SNPshotrs63750161
SNPdbers63750161
MSV3drs63750161
GWAS Ctlgrs63750161
Max Magnitude0
ClinVar
Risk rs63750161(;)
Alt rs63750161(;)
Reference rs63750161(AG;AG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690230_47690231delGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076165.2,