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Rs104894973

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894973
PheGenIrs104894973
nextbiors104894973
hapmaprs104894973
1000 genomesrs104894973
hgdprs104894973
ensemblrs104894973
gopubmedrs104894973
geneviewrs104894973
scholarrs104894973
googlers104894973
pharmgkbrs104894973
gwascentralrs104894973
openSNPrs104894973
23andMers104894973
23andMe allrs104894973
SNP Nexus

SNPshotrs104894973
SNPdbers104894973
MSV3drs104894973
Y Chromrs104894973
GeneSRY
ChromosomeY
Orientationminus
Position2787224
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894973(A;T)
Make rs104894973(T;T)
OMIM480000
Desc
Variant0023
Relatedalso
ClinVar
Risk rs104894973(T;T)
Alt rs104894973(T;T)
Reference rs104894973(A;A)
Significance 5
Disease 46
ClinVar info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
CLNHGVS NC_000024.9:g.2655265T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010410.3