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rs761345398

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs761345398(A;A)
Make rs761345398(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position63483173
GeneACE
is asnp
is mentioned by
dbSNPrs761345398
dbSNP (classic)rs761345398
ClinGenrs761345398
ebirs761345398
HLIrs761345398
Exacrs761345398
Gnomadrs761345398
Varsomers761345398
LitVarrs761345398
Maprs761345398
PheGenIrs761345398
Biobankrs761345398
1000 genomesrs761345398
hgdprs761345398
ensemblrs761345398
geneviewrs761345398
scholarrs761345398
googlers761345398
pharmgkbrs761345398
gwascentralrs761345398
openSNPrs761345398
23andMers761345398
23andMe allrs761345398
SNPshotrs761345398
SNPdbers761345398
MSV3drs761345398
GWAS Ctlgrs761345398
Max Magnitude0
ClinVar
Risk rs761345398(A;A)
Alt rs761345398(A;A)
Reference Rs761345398(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACE
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.61560534G>A
CLNSRC
CLNACC RCV000479383.1,