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rs63750828

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750828(A;A)
Make rs63750828(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47416351
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750828
ebirs63750828
HLIrs63750828
Exacrs63750828
Varsomers63750828
Maprs63750828
PheGenIrs63750828
hapmaprs63750828
1000 genomesrs63750828
hgdprs63750828
ensemblrs63750828
gopubmedrs63750828
geneviewrs63750828
scholarrs63750828
googlers63750828
pharmgkbrs63750828
gwascentralrs63750828
openSNPrs63750828
23andMers63750828
23andMe allrs63750828
SNP Nexus

SNPshotrs63750828
SNPdbers63750828
MSV3drs63750828
GWAS Ctlgrs63750828
Max Magnitude0
ClinVar
Risk rs63750828(A;A)
Alt rs63750828(A;A)
Reference rs63750828(G;G)
Significance Pathogenic
Disease Lynch syndrome not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.47643490G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076778.2, RCV000160579.3, RCV000216069.1,