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Rs104894958

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894958
PheGenIrs104894958
nextbiors104894958
hapmaprs104894958
1000 genomesrs104894958
hgdprs104894958
ensemblrs104894958
gopubmedrs104894958
geneviewrs104894958
scholarrs104894958
googlers104894958
pharmgkbrs104894958
gwascentralrs104894958
openSNPrs104894958
23andMers104894958
23andMe allrs104894958
SNP Nexus

SNPshotrs104894958
SNPdbers104894958
MSV3drs104894958
Y Chromrs104894958
GeneSRY
ChromosomeY
Orientationminus
Position2787327
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894958(C;T)
Make rs104894958(T;T)
OMIM480000
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894958(T;T)
Alt rs104894958(T;T)
Reference rs104894958(C;C)
Significance 5
Disease 46
ClinVar info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
CLNHGVS NC_000024.9:g.2655368G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010393.1