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rs63750261

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750261(C;T)
Make rs63750261(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position5999110
GenePMS2
is asnp
is mentioned by
dbSNPrs63750261
ebirs63750261
HLIrs63750261
Exacrs63750261
Varsomers63750261
Maprs63750261
PheGenIrs63750261
hapmaprs63750261
1000 genomesrs63750261
hgdprs63750261
ensemblrs63750261
gopubmedrs63750261
geneviewrs63750261
scholarrs63750261
googlers63750261
pharmgkbrs63750261
gwascentralrs63750261
openSNPrs63750261
23andMers63750261
23andMe allrs63750261
SNP Nexus

SNPshotrs63750261
SNPdbers63750261
MSV3drs63750261
GWAS Ctlgrs63750261
Max Magnitude0
ClinVar
Risk rs63750261(T;T)
Alt rs63750261(T;T)
Reference rs63750261(C;C)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000007.13:g.6038741G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076882.2, RCV000132294.2,