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rs1057518602

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518602(A;G)
Make rs1057518602(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position104776710
GeneAKT1
is asnp
is mentioned by
dbSNPrs1057518602
dbSNP (old)rs1057518602
ClinGenrs1057518602
ebirs1057518602
HLIrs1057518602
Exacrs1057518602
Gnomadrs1057518602
Varsomers1057518602
Maprs1057518602
PheGenIrs1057518602
Biobankrs1057518602
1000 genomesrs1057518602
hgdprs1057518602
ensemblrs1057518602
gopubmedrs1057518602
geneviewrs1057518602
scholarrs1057518602
googlers1057518602
pharmgkbrs1057518602
gwascentralrs1057518602
openSNPrs1057518602
23andMers1057518602
23andMe allrs1057518602
SNPshotrs1057518602
SNPdbers1057518602
MSV3drs1057518602
GWAS Ctlgrs1057518602
Max Magnitude0
ClinVar
Risk rs1057518602(G;G)
Alt rs1057518602(G;G)
Reference Rs1057518602(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AKT1
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.105243047T>C
CLNSRC
CLNACC RCV000413604.1,