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

rs63750662

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(D;D) 0
Make rs63750662(-;-)
Make rs63750662(-;GA)
Make rs63750662(GA;GA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47466786
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750662
ebirs63750662
HLIrs63750662
Exacrs63750662
Varsomers63750662
Maprs63750662
PheGenIrs63750662
hapmaprs63750662
1000 genomesrs63750662
hgdprs63750662
ensemblrs63750662
gopubmedrs63750662
geneviewrs63750662
scholarrs63750662
googlers63750662
pharmgkbrs63750662
gwascentralrs63750662
openSNPrs63750662
23andMers63750662
23andMe allrs63750662
SNP Nexus

SNPshotrs63750662
SNPdbers63750662
MSV3drs63750662
GWAS Ctlgrs63750662
Max Magnitude0
ClinVar
Risk rs63750662(AG;AG)
Alt rs63750662(AG;AG)
Reference rs63750662(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47693924_47693925dupGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076208.2,