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rs1057521145

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521145(C;T)
Make rs1057521145(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position51789112
GeneSALL4
is asnp
is mentioned by
dbSNPrs1057521145
dbSNP (old)rs1057521145
ClinGenrs1057521145
ebirs1057521145
HLIrs1057521145
Exacrs1057521145
Gnomadrs1057521145
Varsomers1057521145
Maprs1057521145
PheGenIrs1057521145
Biobankrs1057521145
1000 genomesrs1057521145
hgdprs1057521145
ensemblrs1057521145
gopubmedrs1057521145
geneviewrs1057521145
scholarrs1057521145
googlers1057521145
pharmgkbrs1057521145
gwascentralrs1057521145
openSNPrs1057521145
23andMers1057521145
23andMe allrs1057521145
SNPshotrs1057521145
SNPdbers1057521145
MSV3drs1057521145
GWAS Ctlgrs1057521145
Max Magnitude0
ClinVar
Risk rs1057521145(T;T)
Alt rs1057521145(T;T)
Reference Rs1057521145(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SALL4
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.50405651G>A
CLNSRC
CLNACC RCV000417679.1,