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

rs63750501

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATTG;ATTG) 0 common in clinvar
(TGAT;TGAT) 0 common in clinvar
Make rs63750501(-;-)
Make rs63750501(-;ATTG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47408536
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750501
ebirs63750501
HLIrs63750501
Exacrs63750501
Varsomers63750501
Maprs63750501
PheGenIrs63750501
hapmaprs63750501
1000 genomesrs63750501
hgdprs63750501
ensemblrs63750501
gopubmedrs63750501
geneviewrs63750501
scholarrs63750501
googlers63750501
pharmgkbrs63750501
gwascentralrs63750501
openSNPrs63750501
23andMers63750501
23andMe allrs63750501
SNP Nexus

SNPshotrs63750501
SNPdbers63750501
MSV3drs63750501
GWAS Ctlgrs63750501
Max Magnitude0
ClinVar
Risk rs63750501(;)
Alt rs63750501(;)
Reference rs63750501(TGAT;TGAT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47635675_47635678delATTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076569.2,