Rs104894973

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Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894973(A;T)
Make rs104894973(T;T)
ReferenceGRCh38 38.1/141
ChromosomeY
Position2787224
GeneSRY
is asnp
is mentioned by
dbSNPrs104894973
Exacrs104894973
PheGenIrs104894973
nextbiors104894973
hapmaprs104894973
1000 genomesrs104894973
hgdprs104894973
ensemblrs104894973
gopubmedrs104894973
geneviewrs104894973
scholarrs104894973
googlers104894973
pharmgkbrs104894973
gwascentralrs104894973
openSNPrs104894973
23andMers104894973
23andMe allrs104894973
SNP Nexus

SNPshotrs104894973
SNPdbers104894973
MSV3drs104894973
Y Chromrs104894973
OMIM480000
Desc
Variant0023
Relatedalso
ClinVar
Risk rs104894973(T;T)
Alt rs104894973(T;T)
Reference rs104894973(A;A)
Significance Pathogenic
Disease 46
Variation info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
HGVS NC_000024.9:g.2655265T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010410.3,