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rs3209663

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3209663(A;A)
Make rs3209663(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position6005934
GenePMS2
is asnp
is mentioned by
dbSNPrs3209663
ebirs3209663
HLIrs3209663
Exacrs3209663
Varsomers3209663
Maprs3209663
PheGenIrs3209663
hapmaprs3209663
1000 genomesrs3209663
hgdprs3209663
ensemblrs3209663
gopubmedrs3209663
geneviewrs3209663
scholarrs3209663
googlers3209663
pharmgkbrs3209663
gwascentralrs3209663
openSNPrs3209663
23andMers3209663
23andMe allrs3209663
SNP Nexus

SNPshotrs3209663
SNPdbers3209663
MSV3drs3209663
GWAS Ctlgrs3209663
Max Magnitude0
ClinVar
Risk rs3209663(A;A)
Alt rs3209663(A;A)
Reference rs3209663(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6045565C>A
CLNSRC
CLNACC RCV000203898.2,