Rs104894971

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894971
PheGenIrs104894971
nextbiors104894971
hapmaprs104894971
1000 genomesrs104894971
hgdprs104894971
ensemblrs104894971
gopubmedrs104894971
geneviewrs104894971
scholarrs104894971
googlers104894971
pharmgkbrs104894971
gwascentralrs104894971
openSNPrs104894971
23andMers104894971
23andMe allrs104894971
SNP Nexus

SNPshotrs104894971
SNPdbers104894971
MSV3drs104894971
Y Chromrs104894971
GeneSRY
ChromosomeY
Orientationminus
Position2655592
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894971(A;A)
Make rs104894971(A;G)
OMIM480000
Desc
Variant0021
Relatedalso
ClinVar
Risk rs104894971(A;A)
Alt rs104894971(A;A)
Reference rs104894971(G;G)
Significance 5
Disease 46
ClinVar info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
CLNHGVS NC_000024.9:g.2655592C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010408.2