Rs104894956

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894956(C;C)
Make rs104894956(C;T)
ReferenceGRCh38 38.1/141
ChromosomeY
Position2787278
GeneSRY
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
Max Magnitude0
OMIM480000
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894956(C;C)
Alt rs104894956(C;C)
Reference rs104894956(T;T)
Significance Pathogenic
Disease 46
Variation info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
HGVS NC_000024.9:g.2655319A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010391.2,