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rs1064795705

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome7
Position6005891
GenePMS2
is asnp
is mentioned by
dbSNPrs1064795705
dbSNP (old)rs1064795705
ClinGenrs1064795705
ebirs1064795705
HLIrs1064795705
Exacrs1064795705
Gnomadrs1064795705
Varsomers1064795705
LitVarrs1064795705
Maprs1064795705
PheGenIrs1064795705
Biobankrs1064795705
1000 genomesrs1064795705
hgdprs1064795705
ensemblrs1064795705
gopubmedrs1064795705
geneviewrs1064795705
scholarrs1064795705
googlers1064795705
pharmgkbrs1064795705
gwascentralrs1064795705
openSNPrs1064795705
23andMers1064795705
23andMe allrs1064795705
SNPshotrs1064795705
SNPdbers1064795705
MSV3drs1064795705
GWAS Ctlgrs1064795705
Max Magnitude0
ClinVar
Risk rs1064795705(A;A)
Alt rs1064795705(A;A)
Reference Rs1064795705(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PMS2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.6045522C>T
CLNSRC
CLNACC RCV000481277.1,