Have questions? Visit https://www.reddit.com/r/SNPedia

rs63750722

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGG;AAGG) 0 common in clinvar
(AGGA;AGGA) 0 common in clinvar
(D;D) 0
Make rs63750722(-;-)
Make rs63750722(-;AGGA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476521
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750722
ebirs63750722
HLIrs63750722
Exacrs63750722
Varsomers63750722
Maprs63750722
PheGenIrs63750722
hapmaprs63750722
1000 genomesrs63750722
hgdprs63750722
ensemblrs63750722
gopubmedrs63750722
geneviewrs63750722
scholarrs63750722
googlers63750722
pharmgkbrs63750722
gwascentralrs63750722
openSNPrs63750722
23andMers63750722
23andMe allrs63750722
SNP Nexus

SNPshotrs63750722
SNPdbers63750722
MSV3drs63750722
GWAS Ctlgrs63750722
Max Magnitude0
ClinVar
Risk rs63750722(;)
Alt rs63750722(;)
Reference rs63750722(AAGG;AAGG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703660_47703663delAGGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076413.2,