Rs104894971

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894971(A;A)
Make rs104894971(A;G)
ReferenceGRCh38 38.1/141
ChromosomeY
Position2787551
GeneSRY
is asnp
is mentioned by
dbSNPrs104894971
Exacrs104894971
PheGenIrs104894971
nextbiors104894971
hapmaprs104894971
1000 genomesrs104894971
hgdprs104894971
ensemblrs104894971
gopubmedrs104894971
geneviewrs104894971
scholarrs104894971
googlers104894971
pharmgkbrs104894971
gwascentralrs104894971
openSNPrs104894971
23andMers104894971
23andMe allrs104894971
SNP Nexus

SNPshotrs104894971
SNPdbers104894971
MSV3drs104894971
Y Chromrs104894971
Max Magnitude0
OMIM480000
Desc
Variant0021
Relatedalso
ClinVar
Risk rs104894971(A;A)
Alt rs104894971(A;A)
Reference rs104894971(G;G)
Significance Pathogenic
Disease 46
Variation info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
HGVS NC_000024.9:g.2655592C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010408.2,