Rs104894969

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894969(A;A)
Make rs104894969(A;G)
ReferenceGRCh38 38.1/141
ChromosomeY
Position2787412
GeneSRY
is asnp
is mentioned by
dbSNPrs104894969
Exacrs104894969
PheGenIrs104894969
nextbiors104894969
hapmaprs104894969
1000 genomesrs104894969
hgdprs104894969
ensemblrs104894969
gopubmedrs104894969
geneviewrs104894969
scholarrs104894969
googlers104894969
pharmgkbrs104894969
gwascentralrs104894969
openSNPrs104894969
23andMers104894969
23andMe allrs104894969
SNP Nexus

SNPshotrs104894969
SNPdbers104894969
MSV3drs104894969
Y Chromrs104894969
Max Magnitude0
OMIM480000
Desc
Variant0012
Relatedalso
ClinVar
Risk rs104894969(A;A)
Alt rs104894969(A;A)
Reference rs104894969(G;G)
Significance Pathogenic
Disease 46
Variation info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
HGVS NC_000024.9:g.2655453C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010401.1,