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rs878853000

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853000(G;T)
Make rs878853000(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position100746308
GenePAX2
is asnp
is mentioned by
dbSNPrs878853000
ebirs878853000
HLIrs878853000
Exacrs878853000
Varsomers878853000
Maprs878853000
PheGenIrs878853000
hapmaprs878853000
1000 genomesrs878853000
hgdprs878853000
ensemblrs878853000
gopubmedrs878853000
geneviewrs878853000
scholarrs878853000
googlers878853000
pharmgkbrs878853000
gwascentralrs878853000
openSNPrs878853000
23andMers878853000
23andMe allrs878853000
SNP Nexus

SNPshotrs878853000
SNPdbers878853000
MSV3drs878853000
GWAS Ctlgrs878853000
Max Magnitude0
ClinVar
Risk rs878853000(T;T)
Alt rs878853000(T;T)
Reference rs878853000(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PAX2
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.102506065G>T
CLNSRC
CLNACC RCV000224076.1,