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rs63750624

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 6 Lynch syndrome, pathogenic mutation
(G;G) 0 common in clinvar


Make rs63750624(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410211
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750624
dbSNP (classic)rs63750624
ClinGenrs63750624
ebirs63750624
HLIrs63750624
Exacrs63750624
Gnomadrs63750624
Varsomers63750624
LitVarrs63750624
Maprs63750624
PheGenIrs63750624
Biobankrs63750624
1000 genomesrs63750624
hgdprs63750624
ensemblrs63750624
geneviewrs63750624
scholarrs63750624
googlers63750624
pharmgkbrs63750624
gwascentralrs63750624
openSNPrs63750624
23andMers63750624
SNPshotrs63750624
SNPdbers63750624
MSV3drs63750624
GWAS Ctlgrs63750624
Max Magnitude6
ClinVar
Risk rs63750624(A;A)
Alt rs63750624(A;A)
Reference Rs63750624(G;G)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47637350G>A
CLNSRC UniProtKB (protein)
CLNACC RCV000076608.2, RCV000491163.1,