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rs80356379

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0 common in complete genomics
Make rs80356379(-;CGGCAG)
Make rs80356379(CGGCAG;CGGCAG)
ReferenceGRCh38 38.1/141
Chromosome10
Position100750712
GenePAX2
is asnp
is mentioned by
dbSNPrs80356379
ebirs80356379
HLIrs80356379
Exacrs80356379
Varsomers80356379
Maprs80356379
PheGenIrs80356379
hapmaprs80356379
1000 genomesrs80356379
hgdprs80356379
ensemblrs80356379
gopubmedrs80356379
geneviewrs80356379
scholarrs80356379
googlers80356379
pharmgkbrs80356379
gwascentralrs80356379
openSNPrs80356379
23andMers80356379
23andMe allrs80356379
SNP Nexus

SNPshotrs80356379
SNPdbers80356379
MSV3drs80356379
GWAS Ctlgrs80356379
Max Magnitude0
OMIM167409
Desc
Variant0007
Relatedalso
ClinVar
Risk rs80356379(CGGCAG;CGGCAG)
Alt rs80356379(CGGCAG;CGGCAG)
Reference rs80356379(;)
Significance Untested
Disease not provided
Variation info
Gene PAX2
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.102510469_102510470insCGGCAG
CLNSRC ClinVar
CLNACC RCV000144375.1,