Rs104894974

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894974(C;C)
Make rs104894974(C;G)
ReferenceGRCh38 38.1/141
ChromosomeY
Position2787321
GeneSRY
is asnp
is mentioned by
dbSNPrs104894974
Exacrs104894974
PheGenIrs104894974
nextbiors104894974
hapmaprs104894974
1000 genomesrs104894974
hgdprs104894974
ensemblrs104894974
gopubmedrs104894974
geneviewrs104894974
scholarrs104894974
googlers104894974
pharmgkbrs104894974
gwascentralrs104894974
openSNPrs104894974
23andMers104894974
23andMe allrs104894974
SNP Nexus

SNPshotrs104894974
SNPdbers104894974
MSV3drs104894974
Y Chromrs104894974
Max Magnitude0
OMIM480000
Desc
Variant0016
Relatedalso
ClinVar
Risk rs104894974(C;C)
Alt rs104894974(C;C)
Reference rs104894974(G;G)
Significance Pathogenic
Disease 46
Variation info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
HGVS NC_000024.9:g.2655362C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010404.2,