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rs779422412

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779422412(C;T)
Make rs779422412(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position63478093
GeneACE
is asnp
is mentioned by
dbSNPrs779422412
dbSNP (classic)rs779422412
ClinGenrs779422412
ebirs779422412
HLIrs779422412
Exacrs779422412
Gnomadrs779422412
Varsomers779422412
LitVarrs779422412
Maprs779422412
PheGenIrs779422412
Biobankrs779422412
1000 genomesrs779422412
hgdprs779422412
ensemblrs779422412
geneviewrs779422412
scholarrs779422412
googlers779422412
pharmgkbrs779422412
gwascentralrs779422412
openSNPrs779422412
23andMers779422412
23andMe allrs779422412
SNPshotrs779422412
SNPdbers779422412
MSV3drs779422412
GWAS Ctlgrs779422412
Max Magnitude0
ClinVar
Risk rs779422412(T;T)
Alt rs779422412(T;T)
Reference Rs779422412(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ACE
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.61555454C>T
CLNSRC
CLNACC RCV000481663.1,