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rs1057524379

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524379(C;C)
Make rs1057524379(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position72351807
GeneHDAC8
is asnp
is mentioned by
dbSNPrs1057524379
dbSNP (old)rs1057524379
ClinGenrs1057524379
ebirs1057524379
HLIrs1057524379
Exacrs1057524379
Gnomadrs1057524379
Varsomers1057524379
Maprs1057524379
PheGenIrs1057524379
Biobankrs1057524379
1000 genomesrs1057524379
hgdprs1057524379
ensemblrs1057524379
gopubmedrs1057524379
geneviewrs1057524379
scholarrs1057524379
googlers1057524379
pharmgkbrs1057524379
gwascentralrs1057524379
openSNPrs1057524379
23andMers1057524379
23andMe allrs1057524379
SNPshotrs1057524379
SNPdbers1057524379
MSV3drs1057524379
GWAS Ctlgrs1057524379
Max Magnitude0
ClinVar
Risk rs1057524379(C;C)
Alt rs1057524379(C;C)
Reference Rs1057524379(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HDAC8
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.71571657A>G
CLNSRC
CLNACC RCV000422847.1,