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rs1057518019

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518019(C;T)
Make rs1057518019(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position71392681
GeneTAF1
is asnp
is mentioned by
dbSNPrs1057518019
dbSNP (old)rs1057518019
ClinGenrs1057518019
ebirs1057518019
HLIrs1057518019
Exacrs1057518019
Gnomadrs1057518019
Varsomers1057518019
Maprs1057518019
PheGenIrs1057518019
Biobankrs1057518019
1000 genomesrs1057518019
hgdprs1057518019
ensemblrs1057518019
gopubmedrs1057518019
geneviewrs1057518019
scholarrs1057518019
googlers1057518019
pharmgkbrs1057518019
gwascentralrs1057518019
openSNPrs1057518019
23andMers1057518019
23andMe allrs1057518019
SNPshotrs1057518019
SNPdbers1057518019
MSV3drs1057518019
GWAS Ctlgrs1057518019
Max Magnitude0
ClinVar
Risk rs1057518019(T;T)
Alt rs1057518019(T;T)
Reference Rs1057518019(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TAF1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70612531C>T
CLNSRC
CLNACC RCV000413668.1,