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rs63750624

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750624(A;A)
Make rs63750624(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410211
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750624
ebirs63750624
HLIrs63750624
Exacrs63750624
Varsomers63750624
Maprs63750624
PheGenIrs63750624
hapmaprs63750624
1000 genomesrs63750624
hgdprs63750624
ensemblrs63750624
gopubmedrs63750624
geneviewrs63750624
scholarrs63750624
googlers63750624
pharmgkbrs63750624
gwascentralrs63750624
openSNPrs63750624
23andMers63750624
23andMe allrs63750624
SNP Nexus

SNPshotrs63750624
SNPdbers63750624
MSV3drs63750624
GWAS Ctlgrs63750624
Max Magnitude0
ClinVar
Risk rs63750624(A;A)
Alt rs63750624(A;A)
Reference rs63750624(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637350G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076608.2,