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rs1057518131

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518131(C;T)
Make rs1057518131(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position51139068
GeneSALL1
is asnp
is mentioned by
dbSNPrs1057518131
dbSNP (old)rs1057518131
ClinGenrs1057518131
ebirs1057518131
HLIrs1057518131
Exacrs1057518131
Gnomadrs1057518131
Varsomers1057518131
Maprs1057518131
PheGenIrs1057518131
Biobankrs1057518131
1000 genomesrs1057518131
hgdprs1057518131
ensemblrs1057518131
gopubmedrs1057518131
geneviewrs1057518131
scholarrs1057518131
googlers1057518131
pharmgkbrs1057518131
gwascentralrs1057518131
openSNPrs1057518131
23andMers1057518131
23andMe allrs1057518131
SNPshotrs1057518131
SNPdbers1057518131
MSV3drs1057518131
GWAS Ctlgrs1057518131
Max Magnitude0
ClinVar
Risk rs1057518131(T;T)
Alt rs1057518131(T;T)
Reference Rs1057518131(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SALL1
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.51172979G>A
CLNSRC
CLNACC RCV000413349.1,