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rs1064796190

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome7
Position5999158
GenePMS2
is asnp
is mentioned by
dbSNPrs1064796190
dbSNP (classic)rs1064796190
ClinGenrs1064796190
ebirs1064796190
HLIrs1064796190
Exacrs1064796190
Gnomadrs1064796190
Varsomers1064796190
LitVarrs1064796190
Maprs1064796190
PheGenIrs1064796190
Biobankrs1064796190
1000 genomesrs1064796190
hgdprs1064796190
ensemblrs1064796190
geneviewrs1064796190
scholarrs1064796190
googlers1064796190
pharmgkbrs1064796190
gwascentralrs1064796190
openSNPrs1064796190
23andMers1064796190
23andMe allrs1064796190
SNPshotrs1064796190
SNPdbers1064796190
MSV3drs1064796190
GWAS Ctlgrs1064796190
Max Magnitude0
ClinVar
Risk rs1064796190(T;T)
Alt rs1064796190(T;T)
Reference Rs1064796190(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PMS2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.6038789C>A
CLNSRC
CLNACC RCV000479716.1,