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rs1057521722

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521722(C;C)
Make rs1057521722(C;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position53534039
GeneHUWE1
is asnp
is mentioned by
dbSNPrs1057521722
dbSNP (old)rs1057521722
ClinGenrs1057521722
ebirs1057521722
HLIrs1057521722
Exacrs1057521722
Gnomadrs1057521722
Varsomers1057521722
Maprs1057521722
PheGenIrs1057521722
Biobankrs1057521722
1000 genomesrs1057521722
hgdprs1057521722
ensemblrs1057521722
gopubmedrs1057521722
geneviewrs1057521722
scholarrs1057521722
googlers1057521722
pharmgkbrs1057521722
gwascentralrs1057521722
openSNPrs1057521722
23andMers1057521722
23andMe allrs1057521722
SNPshotrs1057521722
SNPdbers1057521722
MSV3drs1057521722
GWAS Ctlgrs1057521722
Max Magnitude0
ClinVar
Risk rs1057521722(C;C)
Alt rs1057521722(C;C)
Reference Rs1057521722(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HUWE1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53561000C>G
CLNSRC
CLNACC RCV000441110.1,