Rs104894958

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Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894958(C;T)
Make rs104894958(T;T)
ReferenceGRCh38 38.1/141
ChromosomeY
Position2787327
GeneSRY
is asnp
is mentioned by
dbSNPrs104894958
Exacrs104894958
PheGenIrs104894958
nextbiors104894958
hapmaprs104894958
1000 genomesrs104894958
hgdprs104894958
ensemblrs104894958
gopubmedrs104894958
geneviewrs104894958
scholarrs104894958
googlers104894958
pharmgkbrs104894958
gwascentralrs104894958
openSNPrs104894958
23andMers104894958
23andMe allrs104894958
SNP Nexus

SNPshotrs104894958
SNPdbers104894958
MSV3drs104894958
Y Chromrs104894958
Max Magnitude0
OMIM480000
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894958(T;T)
Alt rs104894958(T;T)
Reference rs104894958(C;C)
Significance Pathogenic
Disease 46
Variation info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
HGVS NC_000024.9:g.2655368G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010393.1,