Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057517801

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517801(-;-)
Make rs1057517801(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position5987022
GenePMS2
is asnp
is mentioned by
dbSNPrs1057517801
dbSNP (classic)rs1057517801
ClinGenrs1057517801
ebirs1057517801
HLIrs1057517801
Exacrs1057517801
Gnomadrs1057517801
Varsomers1057517801
LitVarrs1057517801
Maprs1057517801
PheGenIrs1057517801
Biobankrs1057517801
1000 genomesrs1057517801
hgdprs1057517801
ensemblrs1057517801
geneviewrs1057517801
scholarrs1057517801
googlers1057517801
pharmgkbrs1057517801
gwascentralrs1057517801
openSNPrs1057517801
23andMers1057517801
23andMe allrs1057517801
SNPshotrs1057517801
SNPdbers1057517801
MSV3drs1057517801
GWAS Ctlgrs1057517801
Max Magnitude0
ClinVar
Risk rs1057517801(-;-)
Alt rs1057517801(-;-)
Reference Rs1057517801(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PMS2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.6026653delT
CLNSRC
CLNACC RCV000412980.1,