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rs1057518216

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518216(C;T)
Make rs1057518216(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position72124037
GeneSOX9
is asnp
is mentioned by
dbSNPrs1057518216
dbSNP (old)rs1057518216
ClinGenrs1057518216
ebirs1057518216
HLIrs1057518216
Exacrs1057518216
Gnomadrs1057518216
Varsomers1057518216
Maprs1057518216
PheGenIrs1057518216
Biobankrs1057518216
1000 genomesrs1057518216
hgdprs1057518216
ensemblrs1057518216
gopubmedrs1057518216
geneviewrs1057518216
scholarrs1057518216
googlers1057518216
pharmgkbrs1057518216
gwascentralrs1057518216
openSNPrs1057518216
23andMers1057518216
23andMe allrs1057518216
SNPshotrs1057518216
SNPdbers1057518216
MSV3drs1057518216
GWAS Ctlgrs1057518216
Max Magnitude0
ClinVar
Risk rs1057518216(T;T)
Alt rs1057518216(T;T)
Reference Rs1057518216(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SOX9
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.70120178C>T
CLNSRC
CLNACC RCV000414443.1,