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rs1057519638

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519638(G;T)
Make rs1057519638(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position842170
GeneDMRT1
is asnp
is mentioned by
dbSNPrs1057519638
dbSNP (classic)rs1057519638
ClinGenrs1057519638
ebirs1057519638
HLIrs1057519638
Exacrs1057519638
Gnomadrs1057519638
Varsomers1057519638
LitVarrs1057519638
Maprs1057519638
PheGenIrs1057519638
Biobankrs1057519638
1000 genomesrs1057519638
hgdprs1057519638
ensemblrs1057519638
geneviewrs1057519638
scholarrs1057519638
googlers1057519638
pharmgkbrs1057519638
gwascentralrs1057519638
openSNPrs1057519638
23andMers1057519638
SNPshotrs1057519638
SNPdbers1057519638
MSV3drs1057519638
GWAS Ctlgrs1057519638
Max Magnitude0
ClinVar
Risk rs1057519638(T;T)
Alt rs1057519638(T;T)
Reference Rs1057519638(G;G)
Significance Probable-Pathogenic
Disease 46
Variation info
Gene DMRT1
CLNDBN 46,XY sex reversal, type 4
Reversed 0
HGVS NC_000009.11:g.842170G>T
CLNSRC
CLNACC RCV000445388.1,