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rs1057518126

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518126(A;A)
Make rs1057518126(A;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position72490962
GeneHDAC8
is asnp
is mentioned by
dbSNPrs1057518126
dbSNP (old)rs1057518126
ClinGenrs1057518126
ebirs1057518126
HLIrs1057518126
Exacrs1057518126
Gnomadrs1057518126
Varsomers1057518126
Maprs1057518126
PheGenIrs1057518126
Biobankrs1057518126
1000 genomesrs1057518126
hgdprs1057518126
ensemblrs1057518126
gopubmedrs1057518126
geneviewrs1057518126
scholarrs1057518126
googlers1057518126
pharmgkbrs1057518126
gwascentralrs1057518126
openSNPrs1057518126
23andMers1057518126
23andMe allrs1057518126
SNPshotrs1057518126
SNPdbers1057518126
MSV3drs1057518126
GWAS Ctlgrs1057518126
Max Magnitude0
ClinVar
Risk rs1057518126(A;A)
Alt rs1057518126(A;A)
Reference Rs1057518126(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HDAC8
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.71710812A>T
CLNSRC
CLNACC RCV000412785.1,