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rs1057518018

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518018(G;T)
Make rs1057518018(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position153932318
GeneNAA10
is asnp
is mentioned by
dbSNPrs1057518018
dbSNP (old)rs1057518018
ClinGenrs1057518018
ebirs1057518018
HLIrs1057518018
Exacrs1057518018
Gnomadrs1057518018
Varsomers1057518018
Maprs1057518018
PheGenIrs1057518018
Biobankrs1057518018
1000 genomesrs1057518018
hgdprs1057518018
ensemblrs1057518018
gopubmedrs1057518018
geneviewrs1057518018
scholarrs1057518018
googlers1057518018
pharmgkbrs1057518018
gwascentralrs1057518018
openSNPrs1057518018
23andMers1057518018
23andMe allrs1057518018
SNPshotrs1057518018
SNPdbers1057518018
MSV3drs1057518018
GWAS Ctlgrs1057518018
Max Magnitude0
ClinVar
Risk rs1057518018(T;T)
Alt rs1057518018(T;T)
Reference Rs1057518018(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NAA10
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153197771C>A
CLNSRC
CLNACC RCV000414189.1,