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rs759151952

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs759151952(-;-)
Make rs759151952(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position5987265
GenePMS2
is asnp
is mentioned by
dbSNPrs759151952
ebirs759151952
HLIrs759151952
Exacrs759151952
Varsomers759151952
Maprs759151952
PheGenIrs759151952
hapmaprs759151952
1000 genomesrs759151952
hgdprs759151952
ensemblrs759151952
gopubmedrs759151952
geneviewrs759151952
scholarrs759151952
googlers759151952
pharmgkbrs759151952
gwascentralrs759151952
openSNPrs759151952
23andMers759151952
23andMe allrs759151952
SNP Nexus

SNPshotrs759151952
SNPdbers759151952
MSV3drs759151952
GWAS Ctlgrs759151952
Max Magnitude0
ClinVar
Risk rs759151952(;)
Alt rs759151952(;)
Reference rs759151952(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000007.13:g.6026896delG
CLNSRC
CLNACC RCV000210104.1,