Rs104894969

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894969
PheGenIrs104894969
nextbiors104894969
hapmaprs104894969
1000 genomesrs104894969
hgdprs104894969
ensemblrs104894969
gopubmedrs104894969
geneviewrs104894969
scholarrs104894969
googlers104894969
pharmgkbrs104894969
gwascentralrs104894969
openSNPrs104894969
23andMers104894969
23andMe allrs104894969
SNP Nexus

SNPshotrs104894969
SNPdbers104894969
MSV3drs104894969
Y Chromrs104894969
GeneSRY
ChromosomeY
Orientationminus
Position2787412
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894969(A;A)
Make rs104894969(A;G)
OMIM480000
Desc
Variant0012
Relatedalso
ClinVar
Risk rs104894969(A;A)
Alt rs104894969(A;A)
Reference rs104894969(G;G)
Significance 5
Disease 46
ClinVar info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
CLNHGVS NC_000024.9:g.2655453C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010401.1