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rs1057521175

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521175(C;C)
Make rs1057521175(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41346910
GeneDDX3X
is asnp
is mentioned by
dbSNPrs1057521175
dbSNP (old)rs1057521175
ClinGenrs1057521175
ebirs1057521175
HLIrs1057521175
Exacrs1057521175
Gnomadrs1057521175
Varsomers1057521175
Maprs1057521175
PheGenIrs1057521175
Biobankrs1057521175
1000 genomesrs1057521175
hgdprs1057521175
ensemblrs1057521175
gopubmedrs1057521175
geneviewrs1057521175
scholarrs1057521175
googlers1057521175
pharmgkbrs1057521175
gwascentralrs1057521175
openSNPrs1057521175
23andMers1057521175
23andMe allrs1057521175
SNPshotrs1057521175
SNPdbers1057521175
MSV3drs1057521175
GWAS Ctlgrs1057521175
Max Magnitude0
ClinVar
Risk rs1057521175(C;C)
Alt rs1057521175(C;C)
Reference Rs1057521175(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41206163T>C
CLNSRC
CLNACC RCV000424111.1,