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rs1057519627

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519627(G;T)
Make rs1057519627(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeY
Position2787377
GeneSRY
is asnp
is mentioned by
dbSNPrs1057519627
dbSNP (old)rs1057519627
ClinGenrs1057519627
ebirs1057519627
HLIrs1057519627
Exacrs1057519627
Gnomadrs1057519627
Varsomers1057519627
LitVarrs1057519627
Maprs1057519627
PheGenIrs1057519627
Biobankrs1057519627
1000 genomesrs1057519627
hgdprs1057519627
ensemblrs1057519627
gopubmedrs1057519627
geneviewrs1057519627
scholarrs1057519627
googlers1057519627
pharmgkbrs1057519627
gwascentralrs1057519627
openSNPrs1057519627
23andMers1057519627
23andMe allrs1057519627
SNPshotrs1057519627
SNPdbers1057519627
MSV3drs1057519627
GWAS Ctlgrs1057519627
Y Chromrs1057519627
Max Magnitude0
ClinVar
Risk rs1057519627(T;T)
Alt rs1057519627(T;T)
Reference Rs1057519627(G;G)
Significance Probable-Pathogenic
Disease 46
Variation info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
HGVS NC_000024.9:g.2655418C>A
CLNSRC
CLNACC RCV000445559.1,