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rs121912703

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912703(C;T)
Make rs121912703(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position63496977
GeneACE
is asnp
is mentioned by
dbSNPrs121912703
ebirs121912703
HLIrs121912703
Exacrs121912703
Varsomers121912703
Maprs121912703
PheGenIrs121912703
hapmaprs121912703
1000 genomesrs121912703
hgdprs121912703
ensemblrs121912703
gopubmedrs121912703
geneviewrs121912703
scholarrs121912703
googlers121912703
pharmgkbrs121912703
gwascentralrs121912703
openSNPrs121912703
23andMers121912703
23andMe allrs121912703
SNP Nexus

SNPshotrs121912703
SNPdbers121912703
MSV3drs121912703
GWAS Ctlgrs121912703
Max Magnitude0
OMIM106180
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121912703(T;T)
Alt rs121912703(T;T)
Reference rs121912703(C;C)
Significance Pathogenic
Disease Angiotensin i-converting enzyme
Variation info
Gene ACE
CLNDBN Angiotensin i-converting enzyme, benign serum increase
Reversed 0
HGVS NC_000017.10:g.61574338C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019685.28,