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rs1057521791

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521791(C;T)
Make rs1057521791(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position53563785
GeneHUWE1
is asnp
is mentioned by
dbSNPrs1057521791
dbSNP (old)rs1057521791
ClinGenrs1057521791
ebirs1057521791
HLIrs1057521791
Exacrs1057521791
Gnomadrs1057521791
Varsomers1057521791
Maprs1057521791
PheGenIrs1057521791
Biobankrs1057521791
1000 genomesrs1057521791
hgdprs1057521791
ensemblrs1057521791
gopubmedrs1057521791
geneviewrs1057521791
scholarrs1057521791
googlers1057521791
pharmgkbrs1057521791
gwascentralrs1057521791
openSNPrs1057521791
23andMers1057521791
23andMe allrs1057521791
SNPshotrs1057521791
SNPdbers1057521791
MSV3drs1057521791
GWAS Ctlgrs1057521791
Max Magnitude0
ClinVar
Risk rs1057521791(T;T)
Alt rs1057521791(T;T)
Reference Rs1057521791(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HUWE1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53590746G>A
CLNSRC
CLNACC RCV000429533.1,