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rs397514688

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514688(C;T)
Make rs397514688(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position63483172
GeneACE
is asnp
is mentioned by
dbSNPrs397514688
ebirs397514688
HLIrs397514688
Exacrs397514688
Varsomers397514688
Maprs397514688
PheGenIrs397514688
hapmaprs397514688
1000 genomesrs397514688
hgdprs397514688
ensemblrs397514688
gopubmedrs397514688
geneviewrs397514688
scholarrs397514688
googlers397514688
pharmgkbrs397514688
gwascentralrs397514688
openSNPrs397514688
23andMers397514688
23andMe allrs397514688
SNP Nexus

SNPshotrs397514688
SNPdbers397514688
MSV3drs397514688
GWAS Ctlgrs397514688
Max Magnitude0
ClinVar
Risk rs397514688(T;T)
Alt rs397514688(T;T)
Reference rs397514688(C;C)
Significance Pathogenic
Disease Renal dysplasia
Variation info
Gene ACE
CLNDBN Renal dysplasia
Reversed 0
HGVS NC_000017.10:g.61560533C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043470.25,