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rs63750396

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750396(A;A)
Make rs63750396(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47416388
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750396
ebirs63750396
HLIrs63750396
Exacrs63750396
Varsomers63750396
Maprs63750396
PheGenIrs63750396
hapmaprs63750396
1000 genomesrs63750396
hgdprs63750396
ensemblrs63750396
gopubmedrs63750396
geneviewrs63750396
scholarrs63750396
googlers63750396
pharmgkbrs63750396
gwascentralrs63750396
openSNPrs63750396
23andMers63750396
23andMe allrs63750396
SNP Nexus

SNPshotrs63750396
SNPdbers63750396
MSV3drs63750396
GWAS Ctlgrs63750396
Max Magnitude0
ClinVar
Risk rs63750396(A;A)
Alt rs63750396(A;A)
Reference rs63750396(G;G)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47643527G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076005.2, RCV000202230.1,