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rs1060503137

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs1060503137(-;-)
Make rs1060503137(-;AT)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position5986900
GenePMS2
is asnp
is mentioned by
dbSNPrs1060503137
dbSNP (old)rs1060503137
ClinGenrs1060503137
ebirs1060503137
HLIrs1060503137
Exacrs1060503137
Gnomadrs1060503137
Varsomers1060503137
LitVarrs1060503137
Maprs1060503137
PheGenIrs1060503137
Biobankrs1060503137
1000 genomesrs1060503137
hgdprs1060503137
ensemblrs1060503137
gopubmedrs1060503137
geneviewrs1060503137
scholarrs1060503137
googlers1060503137
pharmgkbrs1060503137
gwascentralrs1060503137
openSNPrs1060503137
23andMers1060503137
23andMe allrs1060503137
SNPshotrs1060503137
SNPdbers1060503137
MSV3drs1060503137
GWAS Ctlgrs1060503137
Max Magnitude0
ClinVar
Risk rs1060503137(-;-)
Alt rs1060503137(-;-)
Reference Rs1060503137(AT;AT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome
Reversed 1
HGVS NC_000007.13:g.6026531_6026532delAT
CLNSRC
CLNACC RCV000469787.1,