Rs104894972

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894972(A;A)
Make rs104894972(A;G)
ReferenceGRCh38 38.1/141
ChromosomeY
Position2787320
GeneSRY
is asnp
is mentioned by
dbSNPrs104894972
Exacrs104894972
PheGenIrs104894972
nextbiors104894972
hapmaprs104894972
1000 genomesrs104894972
hgdprs104894972
ensemblrs104894972
gopubmedrs104894972
geneviewrs104894972
scholarrs104894972
googlers104894972
pharmgkbrs104894972
gwascentralrs104894972
openSNPrs104894972
23andMers104894972
23andMe allrs104894972
SNP Nexus

SNPshotrs104894972
SNPdbers104894972
MSV3drs104894972
Y Chromrs104894972
Max Magnitude0
OMIM480000
Desc
Variant0022
Relatedalso
ClinVar
Risk rs104894972(A;A)
Alt rs104894972(A;A)
Reference rs104894972(G;G)
Significance Pathogenic
Disease 46
Variation info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
HGVS NC_000024.9:g.2655361C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010409.1,