Rs104894975

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894975
PheGenIrs104894975
nextbiors104894975
hapmaprs104894975
1000 genomesrs104894975
hgdprs104894975
ensemblrs104894975
gopubmedrs104894975
geneviewrs104894975
scholarrs104894975
googlers104894975
pharmgkbrs104894975
gwascentralrs104894975
openSNPrs104894975
23andMers104894975
23andMe allrs104894975
SNP Nexus

SNPshotrs104894975
SNPdbers104894975
MSV3drs104894975
Y Chromrs104894975
GeneSRY
ChromosomeY
Orientationminus
Position2655633
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894975(A;A)
Make rs104894975(A;T)
OMIM480000
Desc
Variant0018
Relatedalso
ClinVar
Risk rs104894975(A;A)
Alt rs104894975(A;A)
Reference rs104894975(T;T)
Significance 5
Disease 46
ClinVar info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
CLNHGVS NC_000024.9:g.2655633A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010405.3