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rs767354861

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs767354861(C;T)
Make rs767354861(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position71375242
GeneTAF1
is asnp
is mentioned by
dbSNPrs767354861
dbSNP (classic)rs767354861
ClinGenrs767354861
ebirs767354861
HLIrs767354861
Exacrs767354861
Gnomadrs767354861
Varsomers767354861
LitVarrs767354861
Maprs767354861
PheGenIrs767354861
Biobankrs767354861
1000 genomesrs767354861
hgdprs767354861
ensemblrs767354861
geneviewrs767354861
scholarrs767354861
googlers767354861
pharmgkbrs767354861
gwascentralrs767354861
openSNPrs767354861
23andMers767354861
SNPshotrs767354861
SNPdbers767354861
MSV3drs767354861
GWAS Ctlgrs767354861
Max Magnitude0
ClinVar
Risk rs767354861(T;T)
Alt rs767354861(T;T)
Reference Rs767354861(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TAF1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70595092C>T
CLNSRC
CLNACC RCV000427808.1,