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rs1057518264

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518264(A;A)
Make rs1057518264(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position53314796
GeneAAAS
is asnp
is mentioned by
dbSNPrs1057518264
dbSNP (old)rs1057518264
ClinGenrs1057518264
ebirs1057518264
HLIrs1057518264
Exacrs1057518264
Gnomadrs1057518264
Varsomers1057518264
Maprs1057518264
PheGenIrs1057518264
Biobankrs1057518264
1000 genomesrs1057518264
hgdprs1057518264
ensemblrs1057518264
gopubmedrs1057518264
geneviewrs1057518264
scholarrs1057518264
googlers1057518264
pharmgkbrs1057518264
gwascentralrs1057518264
openSNPrs1057518264
23andMers1057518264
23andMe allrs1057518264
SNPshotrs1057518264
SNPdbers1057518264
MSV3drs1057518264
GWAS Ctlgrs1057518264
Max Magnitude0
ClinVar
Risk rs1057518264(A;A)
Alt rs1057518264(A;A)
Reference Rs1057518264(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AAAS
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.53708580G>T
CLNSRC
CLNACC RCV000413311.1,