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rs876661042

From SNPedia

Orientationminus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs876661042(-;-)
Make rs876661042(-;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position5973487
GenePMS2
is asnp
is mentioned by
dbSNPrs876661042
ebirs876661042
HLIrs876661042
Exacrs876661042
Varsomers876661042
Maprs876661042
PheGenIrs876661042
hapmaprs876661042
1000 genomesrs876661042
hgdprs876661042
ensemblrs876661042
gopubmedrs876661042
geneviewrs876661042
scholarrs876661042
googlers876661042
pharmgkbrs876661042
gwascentralrs876661042
openSNPrs876661042
23andMers876661042
23andMe allrs876661042
SNP Nexus

SNPshotrs876661042
SNPdbers876661042
MSV3drs876661042
GWAS Ctlgrs876661042
Max Magnitude0
ClinVar
Risk rs876661042(;)
Alt rs876661042(;)
Reference rs876661042(AT;AT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PMS2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.6013118_6013119delAT
CLNSRC
CLNACC RCV000222715.1,