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rs1064794152

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome7
Position6005939
GenePMS2
is asnp
is mentioned by
dbSNPrs1064794152
dbSNP (classic)rs1064794152
ClinGenrs1064794152
ebirs1064794152
HLIrs1064794152
Exacrs1064794152
Gnomadrs1064794152
Varsomers1064794152
LitVarrs1064794152
Maprs1064794152
PheGenIrs1064794152
Biobankrs1064794152
1000 genomesrs1064794152
hgdprs1064794152
ensemblrs1064794152
geneviewrs1064794152
scholarrs1064794152
googlers1064794152
pharmgkbrs1064794152
gwascentralrs1064794152
openSNPrs1064794152
23andMers1064794152
23andMe allrs1064794152
SNPshotrs1064794152
SNPdbers1064794152
MSV3drs1064794152
GWAS Ctlgrs1064794152
Max Magnitude0
ClinVar
Risk rs1064794152(-;-)
Alt rs1064794152(-;-)
Reference Rs1064794152(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PMS2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.6045570delA
CLNSRC
CLNACC RCV000483540.1,