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rs745487791

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs745487791(C;C)
Make rs745487791(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position5997425
GenePMS2
is asnp
is mentioned by
dbSNPrs745487791
ebirs745487791
HLIrs745487791
Exacrs745487791
Varsomers745487791
Maprs745487791
PheGenIrs745487791
hapmaprs745487791
1000 genomesrs745487791
hgdprs745487791
ensemblrs745487791
gopubmedrs745487791
geneviewrs745487791
scholarrs745487791
googlers745487791
pharmgkbrs745487791
gwascentralrs745487791
openSNPrs745487791
23andMers745487791
23andMe allrs745487791
SNP Nexus

SNPshotrs745487791
SNPdbers745487791
MSV3drs745487791
GWAS Ctlgrs745487791
Max Magnitude0
ClinVar
Risk rs745487791(A,C,G;A,C,G)
Alt rs745487791(A,C,G;A,C,G)
Reference rs745487791(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PMS2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000007.13:g.6037056T>G
CLNSRC
CLNACC RCV000165791.1,