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rs63751228

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751228(C;T)
Make rs63751228(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position5987354
GenePMS2
is asnp
is mentioned by
dbSNPrs63751228
ebirs63751228
HLIrs63751228
Exacrs63751228
Varsomers63751228
Maprs63751228
PheGenIrs63751228
hapmaprs63751228
1000 genomesrs63751228
hgdprs63751228
ensemblrs63751228
gopubmedrs63751228
geneviewrs63751228
scholarrs63751228
googlers63751228
pharmgkbrs63751228
gwascentralrs63751228
openSNPrs63751228
23andMers63751228
23andMe allrs63751228
SNP Nexus

SNPshotrs63751228
SNPdbers63751228
MSV3drs63751228
GWAS Ctlgrs63751228
Max Magnitude0
ClinVar
Risk rs63751228(T;T)
Alt rs63751228(T;T)
Reference rs63751228(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PMS2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000007.13:g.6026985G>A
CLNSRC
CLNACC RCV000166728.1,