Rs104894956

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894956
PheGenIrs104894956
nextbiors104894956
hapmaprs104894956
1000 genomesrs104894956
hgdprs104894956
ensemblrs104894956
gopubmedrs104894956
geneviewrs104894956
scholarrs104894956
googlers104894956
pharmgkbrs104894956
gwascentralrs104894956
openSNPrs104894956
23andMers104894956
23andMe allrs104894956
SNP Nexus

SNPshotrs104894956
SNPdbers104894956
MSV3drs104894956
Y Chromrs104894956
GeneSRY
ChromosomeY
Orientationminus
Position2655319
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894956(C;C)
Make rs104894956(C;T)
OMIM480000
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894956(C;C)
Alt rs104894956(C;C)
Reference rs104894956(T;T)
Significance 5
Disease 46
ClinVar info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
CLNHGVS NC_000024.9:g.2655319A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010391.2