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rs747453876

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs747453876(C;C)
Make rs747453876(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position100787013
GenePAX2
is asnp
is mentioned by
dbSNPrs747453876
dbSNP (classic)rs747453876
ClinGenrs747453876
ebirs747453876
HLIrs747453876
Exacrs747453876
Gnomadrs747453876
Varsomers747453876
LitVarrs747453876
Maprs747453876
PheGenIrs747453876
Biobankrs747453876
1000 genomesrs747453876
hgdprs747453876
ensemblrs747453876
geneviewrs747453876
scholarrs747453876
googlers747453876
pharmgkbrs747453876
gwascentralrs747453876
openSNPrs747453876
23andMers747453876
23andMe allrs747453876
SNPshotrs747453876
SNPdbers747453876
MSV3drs747453876
GWAS Ctlgrs747453876
Max Magnitude0
ClinVar
Risk rs747453876(C;C)
Alt rs747453876(C;C)
Reference Rs747453876(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PAX2
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.102546770T>C
CLNSRC
CLNACC RCV000483686.1,