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rs387906576

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TGGA;TGGA) 0 common in clinvar
Make rs387906576(-;-)
Make rs387906576(-;TGGA)
ReferenceGRCh38 38.1/141
Chromosome17
Position63482666
GeneACE
is asnp
is mentioned by
dbSNPrs387906576
ebirs387906576
HLIrs387906576
Exacrs387906576
Varsomers387906576
Maprs387906576
PheGenIrs387906576
hapmaprs387906576
1000 genomesrs387906576
hgdprs387906576
ensemblrs387906576
gopubmedrs387906576
geneviewrs387906576
scholarrs387906576
googlers387906576
pharmgkbrs387906576
gwascentralrs387906576
openSNPrs387906576
23andMers387906576
23andMe allrs387906576
SNP Nexus

SNPshotrs387906576
SNPdbers387906576
MSV3drs387906576
GWAS Ctlgrs387906576
Max Magnitude0
ClinVar
Risk rs387906576(;)
Alt rs387906576(;)
Reference rs387906576(TGGA;TGGA)
Significance Pathogenic
Disease Renal dysplasia
Variation info
Gene ACE
CLNDBN Renal dysplasia
Reversed 0
HGVS NC_000017.10:g.61560027_61560030delTGGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000019687.27,