Rs104894970

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Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894970(A;T)
Make rs104894970(T;T)
ReferenceGRCh38 38.1/141
ChromosomeY
Position2787330
GeneSRY
is asnp
is mentioned by
dbSNPrs104894970
Exacrs104894970
PheGenIrs104894970
nextbiors104894970
hapmaprs104894970
1000 genomesrs104894970
hgdprs104894970
ensemblrs104894970
gopubmedrs104894970
geneviewrs104894970
scholarrs104894970
googlers104894970
pharmgkbrs104894970
gwascentralrs104894970
openSNPrs104894970
23andMers104894970
23andMe allrs104894970
SNP Nexus

SNPshotrs104894970
SNPdbers104894970
MSV3drs104894970
Y Chromrs104894970
OMIM480000
Desc
Variant0015
Relatedalso
ClinVar
Risk rs104894970(T;T)
Alt rs104894970(T;T)
Reference rs104894970(A;A)
Significance Pathogenic
Disease 46
Variation info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
HGVS NC_000024.9:g.2655371T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010403.3,