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

rs63750330

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750330(C;C)
Make rs63750330(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47466710
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750330
ebirs63750330
HLIrs63750330
Exacrs63750330
Varsomers63750330
Maprs63750330
PheGenIrs63750330
hapmaprs63750330
1000 genomesrs63750330
hgdprs63750330
ensemblrs63750330
gopubmedrs63750330
geneviewrs63750330
scholarrs63750330
googlers63750330
pharmgkbrs63750330
gwascentralrs63750330
openSNPrs63750330
23andMers63750330
23andMe allrs63750330
SNP Nexus

SNPshotrs63750330
SNPdbers63750330
MSV3drs63750330
GWAS Ctlgrs63750330
Max Magnitude0
ClinVar
Risk rs63750330(C;C)
Alt rs63750330(C;C)
Reference rs63750330(T;T)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000002.11:g.47693849T>A; NC_000002.11:g.47693849T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000205506.1, RCV000076194.3, RCV000126814.5, RCV000212604.1,