Rs104894972

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894972
PheGenIrs104894972
nextbiors104894972
hapmaprs104894972
1000 genomesrs104894972
hgdprs104894972
ensemblrs104894972
gopubmedrs104894972
geneviewrs104894972
scholarrs104894972
googlers104894972
pharmgkbrs104894972
gwascentralrs104894972
openSNPrs104894972
23andMers104894972
23andMe allrs104894972
SNP Nexus

SNPshotrs104894972
SNPdbers104894972
MSV3drs104894972
Y Chromrs104894972
GeneSRY
ChromosomeY
Orientationminus
Position2655361
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894972(A;A)
Make rs104894972(A;G)
OMIM480000
Desc
Variant0022
Relatedalso
ClinVar
Risk rs104894972(A;A)
Alt rs104894972(A;A)
Reference rs104894972(G;G)
Significance 5
Disease 46
ClinVar info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
CLNHGVS NC_000024.9:g.2655361C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010409.1