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rs1057518047

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518047(G;T)
Make rs1057518047(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position72567907
GeneHDAC8
is asnp
is mentioned by
dbSNPrs1057518047
dbSNP (old)rs1057518047
ClinGenrs1057518047
ebirs1057518047
HLIrs1057518047
Exacrs1057518047
Gnomadrs1057518047
Varsomers1057518047
Maprs1057518047
PheGenIrs1057518047
Biobankrs1057518047
1000 genomesrs1057518047
hgdprs1057518047
ensemblrs1057518047
gopubmedrs1057518047
geneviewrs1057518047
scholarrs1057518047
googlers1057518047
pharmgkbrs1057518047
gwascentralrs1057518047
openSNPrs1057518047
23andMers1057518047
23andMe allrs1057518047
SNPshotrs1057518047
SNPdbers1057518047
MSV3drs1057518047
GWAS Ctlgrs1057518047
Max Magnitude0
ClinVar
Risk rs1057518047(T;T)
Alt rs1057518047(T;T)
Reference Rs1057518047(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HDAC8
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.71787757C>A
CLNSRC
CLNACC RCV000413537.1,