Rs104894975

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894975(A;A)
Make rs104894975(A;T)
ReferenceGRCh38 38.1/141
ChromosomeY
Position2787592
GeneSRY
is asnp
is mentioned by
dbSNPrs104894975
Exacrs104894975
PheGenIrs104894975
nextbiors104894975
hapmaprs104894975
1000 genomesrs104894975
hgdprs104894975
ensemblrs104894975
gopubmedrs104894975
geneviewrs104894975
scholarrs104894975
googlers104894975
pharmgkbrs104894975
gwascentralrs104894975
openSNPrs104894975
23andMers104894975
23andMe allrs104894975
SNP Nexus

SNPshotrs104894975
SNPdbers104894975
MSV3drs104894975
Y Chromrs104894975
Max Magnitude0
OMIM480000
Desc
Variant0018
Relatedalso
ClinVar
Risk rs104894975(A;A)
Alt rs104894975(A;A)
Reference rs104894975(T;T)
Significance Pathogenic
Disease 46
Variation info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
HGVS NC_000024.9:g.2655633A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010405.3,