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rs63750149

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(I;I) 0
Make rs63750149(-;-)
Make rs63750149(-;A)
Make rs63750149(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478396
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750149
ebirs63750149
HLIrs63750149
Exacrs63750149
Varsomers63750149
Maprs63750149
PheGenIrs63750149
hapmaprs63750149
1000 genomesrs63750149
hgdprs63750149
ensemblrs63750149
gopubmedrs63750149
geneviewrs63750149
scholarrs63750149
googlers63750149
pharmgkbrs63750149
gwascentralrs63750149
openSNPrs63750149
23andMers63750149
23andMe allrs63750149
SNP Nexus

SNPshotrs63750149
SNPdbers63750149
MSV3drs63750149
GWAS Ctlgrs63750149
Max Magnitude0
ClinVar
Risk rs63750149(A;A)
Alt rs63750149(A;A)
Reference rs63750149(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705535dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076459.2,