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rs587777708

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777708(A;A)
Make rs587777708(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position100749869
GenePAX2
is asnp
is mentioned by
dbSNPrs587777708
ebirs587777708
HLIrs587777708
Exacrs587777708
Varsomers587777708
Maprs587777708
PheGenIrs587777708
hapmaprs587777708
1000 genomesrs587777708
hgdprs587777708
ensemblrs587777708
gopubmedrs587777708
geneviewrs587777708
scholarrs587777708
googlers587777708
pharmgkbrs587777708
gwascentralrs587777708
openSNPrs587777708
23andMers587777708
23andMe allrs587777708
SNP Nexus

SNPshotrs587777708
SNPdbers587777708
MSV3drs587777708
GWAS Ctlgrs587777708
Max Magnitude0
ClinVar
Risk rs587777708(A;A)
Alt rs587777708(A;A)
Reference rs587777708(G;G)
Significance Pathogenic
Disease Focal segmental glomerulosclerosis 7
Variation info
Gene PAX2
CLNDBN Focal segmental glomerulosclerosis 7
Reversed 0
HGVS NC_000010.10:g.102509626G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144051.2,