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rs63750786

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63750786(-;-)
Make rs63750786(-;G)
Make rs63750786(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410319
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750786
ebirs63750786
HLIrs63750786
Exacrs63750786
Varsomers63750786
Maprs63750786
PheGenIrs63750786
hapmaprs63750786
1000 genomesrs63750786
hgdprs63750786
ensemblrs63750786
gopubmedrs63750786
geneviewrs63750786
scholarrs63750786
googlers63750786
pharmgkbrs63750786
gwascentralrs63750786
openSNPrs63750786
23andMers63750786
23andMe allrs63750786
SNP Nexus

SNPshotrs63750786
SNPdbers63750786
MSV3drs63750786
GWAS Ctlgrs63750786
Max Magnitude0
ClinVar
Risk rs63750786(G;G)
Alt rs63750786(G;G)
Reference rs63750786(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637458dupG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076648.2,