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rs63750466

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750466(A;A)
Make rs63750466(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47403195
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750466
ebirs63750466
HLIrs63750466
Exacrs63750466
Varsomers63750466
Maprs63750466
PheGenIrs63750466
hapmaprs63750466
1000 genomesrs63750466
hgdprs63750466
ensemblrs63750466
gopubmedrs63750466
geneviewrs63750466
scholarrs63750466
googlers63750466
pharmgkbrs63750466
gwascentralrs63750466
openSNPrs63750466
23andMers63750466
23andMe allrs63750466
SNP Nexus

SNPshotrs63750466
SNPdbers63750466
MSV3drs63750466
GWAS Ctlgrs63750466
Max Magnitude0
ClinVar
Risk rs63750466(A;A)
Alt rs63750466(A;A)
Reference rs63750466(G;G)
Significance Probable-non-pathogenic
Disease not provided Lynch syndrome I Hereditary cancer-predisposing syndrome not specified Lynch syndrome
Variation info
Gene MSH2
CLNDBN not provided Lynch syndrome I Hereditary cancer-predisposing syndrome not specified Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47630334G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000034558.1, RCV000076617.3, RCV000115534.5, RCV000202071.1, RCV000206355.2,