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rs587782704

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782704(-;-)
Make rs587782704(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position5982881
GenePMS2
is asnp
is mentioned by
dbSNPrs587782704
ebirs587782704
HLIrs587782704
Exacrs587782704
Varsomers587782704
Maprs587782704
PheGenIrs587782704
hapmaprs587782704
1000 genomesrs587782704
hgdprs587782704
ensemblrs587782704
gopubmedrs587782704
geneviewrs587782704
scholarrs587782704
googlers587782704
pharmgkbrs587782704
gwascentralrs587782704
openSNPrs587782704
23andMers587782704
23andMe allrs587782704
SNP Nexus

SNPshotrs587782704
SNPdbers587782704
MSV3drs587782704
GWAS Ctlgrs587782704
Max Magnitude0
ClinVar
Risk rs587782704(;)
Alt rs587782704(;)
Reference rs587782704(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Lynch syndrome
Variation info
Gene PMS2
CLNDBN Hereditary cancer-predisposing syndrome not provided Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6022512delT
CLNSRC
CLNACC RCV000132155.2, RCV000221406.1, RCV000228992.1,