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rs1057518232

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518232(-;C)
Make rs1057518232(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position51140458
GeneSALL1
is asnp
is mentioned by
dbSNPrs1057518232
dbSNP (old)rs1057518232
ClinGenrs1057518232
ebirs1057518232
HLIrs1057518232
Exacrs1057518232
Gnomadrs1057518232
Varsomers1057518232
Maprs1057518232
PheGenIrs1057518232
Biobankrs1057518232
1000 genomesrs1057518232
hgdprs1057518232
ensemblrs1057518232
gopubmedrs1057518232
geneviewrs1057518232
scholarrs1057518232
googlers1057518232
pharmgkbrs1057518232
gwascentralrs1057518232
openSNPrs1057518232
23andMers1057518232
23andMe allrs1057518232
SNPshotrs1057518232
SNPdbers1057518232
MSV3drs1057518232
GWAS Ctlgrs1057518232
Max Magnitude0
ClinVar
Risk rs1057518232(C;C)
Alt rs1057518232(C;C)
Reference Rs1057518232(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene SALL1
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.51174370dupG
CLNSRC
CLNACC RCV000414487.1,