Rs104894970

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894970
PheGenIrs104894970
nextbiors104894970
hapmaprs104894970
1000 genomesrs104894970
hgdprs104894970
ensemblrs104894970
gopubmedrs104894970
geneviewrs104894970
scholarrs104894970
googlers104894970
pharmgkbrs104894970
gwascentralrs104894970
openSNPrs104894970
23andMers104894970
23andMe allrs104894970
SNP Nexus

SNPshotrs104894970
SNPdbers104894970
MSV3drs104894970
Y Chromrs104894970
GeneSRY
ChromosomeY
Orientationminus
Position2787330
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894970(A;T)
Make rs104894970(T;T)
OMIM480000
Desc
Variant0015
Relatedalso
ClinVar
Risk rs104894970(T;T)
Alt rs104894970(T;T)
Reference rs104894970(A;A)
Significance 5
Disease 46
ClinVar info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
CLNHGVS NC_000024.9:g.2655371T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010403.3