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rs63750477

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750477(-;-)
Make rs63750477(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position5986997
GenePMS2
is asnp
is mentioned by
dbSNPrs63750477
ebirs63750477
HLIrs63750477
Exacrs63750477
Varsomers63750477
Maprs63750477
PheGenIrs63750477
hapmaprs63750477
1000 genomesrs63750477
hgdprs63750477
ensemblrs63750477
gopubmedrs63750477
geneviewrs63750477
scholarrs63750477
googlers63750477
pharmgkbrs63750477
gwascentralrs63750477
openSNPrs63750477
23andMers63750477
23andMe allrs63750477
SNP Nexus

SNPshotrs63750477
SNPdbers63750477
MSV3drs63750477
GWAS Ctlgrs63750477
Max Magnitude0
ClinVar
Risk rs63750477(;)
Alt rs63750477(;)
Reference rs63750477(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6026628delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076826.2,