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rs1057518273

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518273(C;T)
Make rs1057518273(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position51140829
GeneSALL1
is asnp
is mentioned by
dbSNPrs1057518273
dbSNP (old)rs1057518273
ClinGenrs1057518273
ebirs1057518273
HLIrs1057518273
Exacrs1057518273
Gnomadrs1057518273
Varsomers1057518273
Maprs1057518273
PheGenIrs1057518273
Biobankrs1057518273
1000 genomesrs1057518273
hgdprs1057518273
ensemblrs1057518273
gopubmedrs1057518273
geneviewrs1057518273
scholarrs1057518273
googlers1057518273
pharmgkbrs1057518273
gwascentralrs1057518273
openSNPrs1057518273
23andMers1057518273
23andMe allrs1057518273
SNPshotrs1057518273
SNPdbers1057518273
MSV3drs1057518273
GWAS Ctlgrs1057518273
Max Magnitude0
ClinVar
Risk rs1057518273(T;T)
Alt rs1057518273(T;T)
Reference Rs1057518273(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SALL1
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.51174740G>A
CLNSRC
CLNACC RCV000414232.1,