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Rs104894974

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894974
PheGenIrs104894974
nextbiors104894974
hapmaprs104894974
1000 genomesrs104894974
hgdprs104894974
ensemblrs104894974
gopubmedrs104894974
geneviewrs104894974
scholarrs104894974
googlers104894974
pharmgkbrs104894974
gwascentralrs104894974
openSNPrs104894974
23andMers104894974
23andMe allrs104894974
SNP Nexus

SNPshotrs104894974
SNPdbers104894974
MSV3drs104894974
Y Chromrs104894974
GeneSRY
ChromosomeY
Orientationminus
Position2787321
ReferenceGRCh38 38.1/141
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894974(C;C)
Make rs104894974(C;G)
OMIM480000
Desc
Variant0016
Relatedalso
ClinVar
Risk rs104894974(C;C)
Alt rs104894974(C;C)
Reference rs104894974(G;G)
Significance 5
Disease 46
ClinVar info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
CLNHGVS NC_000024.9:g.2655362C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010404.2