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rs876661203

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661203(A;A)
Make rs876661203(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position5973466
GenePMS2
is asnp
is mentioned by
dbSNPrs876661203
ebirs876661203
HLIrs876661203
Exacrs876661203
Varsomers876661203
Maprs876661203
PheGenIrs876661203
hapmaprs876661203
1000 genomesrs876661203
hgdprs876661203
ensemblrs876661203
gopubmedrs876661203
geneviewrs876661203
scholarrs876661203
googlers876661203
pharmgkbrs876661203
gwascentralrs876661203
openSNPrs876661203
23andMers876661203
23andMe allrs876661203
SNP Nexus

SNPshotrs876661203
SNPdbers876661203
MSV3drs876661203
GWAS Ctlgrs876661203
Max Magnitude0
ClinVar
Risk rs876661203(A;A)
Alt rs876661203(A;A)
Reference rs876661203(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PMS2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.6013097C>T
CLNSRC
CLNACC RCV000217259.1,