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rs778390161

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs778390161(A;A)
Make rs778390161(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position63490953
GeneACE
is asnp
is mentioned by
dbSNPrs778390161
dbSNP (classic)rs778390161
ClinGenrs778390161
ebirs778390161
HLIrs778390161
Exacrs778390161
Gnomadrs778390161
Varsomers778390161
LitVarrs778390161
Maprs778390161
PheGenIrs778390161
Biobankrs778390161
1000 genomesrs778390161
hgdprs778390161
ensemblrs778390161
geneviewrs778390161
scholarrs778390161
googlers778390161
pharmgkbrs778390161
gwascentralrs778390161
openSNPrs778390161
23andMers778390161
23andMe allrs778390161
SNPshotrs778390161
SNPdbers778390161
MSV3drs778390161
GWAS Ctlgrs778390161
Max Magnitude0
ClinVar
Risk rs778390161(A;A)
Alt rs778390161(A;A)
Reference Rs778390161(G;G)
Significance Probable-Pathogenic
Disease Renal dysplasia
Variation info
Gene ACE
CLNDBN Renal dysplasia
Reversed 0
HGVS NC_000017.10:g.61568314G>A
CLNSRC
CLNACC RCV000416335.1,