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rs1057518605

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518605(C;C)
Make rs1057518605(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position153930794
GeneNAA10
is asnp
is mentioned by
dbSNPrs1057518605
dbSNP (old)rs1057518605
ClinGenrs1057518605
ebirs1057518605
HLIrs1057518605
Exacrs1057518605
Gnomadrs1057518605
Varsomers1057518605
Maprs1057518605
PheGenIrs1057518605
Biobankrs1057518605
1000 genomesrs1057518605
hgdprs1057518605
ensemblrs1057518605
gopubmedrs1057518605
geneviewrs1057518605
scholarrs1057518605
googlers1057518605
pharmgkbrs1057518605
gwascentralrs1057518605
openSNPrs1057518605
23andMers1057518605
23andMe allrs1057518605
SNPshotrs1057518605
SNPdbers1057518605
MSV3drs1057518605
GWAS Ctlgrs1057518605
Max Magnitude0
ClinVar
Risk rs1057518605(C;C)
Alt rs1057518605(C;C)
Reference Rs1057518605(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NAA10
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153196247A>G
CLNSRC
CLNACC RCV000414408.1,