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rs747815674

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs747815674(A;A)
Make rs747815674(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position230709994
GeneAGT
is asnp
is mentioned by
dbSNPrs747815674
dbSNP (classic)rs747815674
ClinGenrs747815674
ebirs747815674
HLIrs747815674
Exacrs747815674
Gnomadrs747815674
Varsomers747815674
LitVarrs747815674
Maprs747815674
PheGenIrs747815674
Biobankrs747815674
1000 genomesrs747815674
hgdprs747815674
ensemblrs747815674
geneviewrs747815674
scholarrs747815674
googlers747815674
pharmgkbrs747815674
gwascentralrs747815674
openSNPrs747815674
23andMers747815674
23andMe allrs747815674
SNPshotrs747815674
SNPdbers747815674
MSV3drs747815674
GWAS Ctlgrs747815674
Max Magnitude0
ClinVar
Risk rs747815674(A;A)
Alt rs747815674(A;A)
Reference Rs747815674(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene AGT
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.230845740C>A
CLNSRC
CLNACC RCV000493969.1,