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rs766389591

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs766389591(-;-)
Make rs766389591(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position5986987
GenePMS2
is asnp
is mentioned by
dbSNPrs766389591
ebirs766389591
HLIrs766389591
Exacrs766389591
Varsomers766389591
Maprs766389591
PheGenIrs766389591
hapmaprs766389591
1000 genomesrs766389591
hgdprs766389591
ensemblrs766389591
gopubmedrs766389591
geneviewrs766389591
scholarrs766389591
googlers766389591
pharmgkbrs766389591
gwascentralrs766389591
openSNPrs766389591
23andMers766389591
23andMe allrs766389591
SNP Nexus

SNPshotrs766389591
SNPdbers766389591
MSV3drs766389591
GWAS Ctlgrs766389591
Max Magnitude0
ClinVar
Risk rs766389591(;)
Alt rs766389591(;)
Reference rs766389591(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PMS2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.6026618delT
CLNSRC
CLNACC RCV000217805.1,