Rs104894957

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894957
PheGenIrs104894957
nextbiors104894957
hapmaprs104894957
1000 genomesrs104894957
hgdprs104894957
ensemblrs104894957
gopubmedrs104894957
geneviewrs104894957
scholarrs104894957
googlers104894957
pharmgkbrs104894957
gwascentralrs104894957
openSNPrs104894957
23andMers104894957
23andMe allrs104894957
SNP Nexus

SNPshotrs104894957
SNPdbers104894957
MSV3drs104894957
Y Chromrs104894957
GeneSRY
ChromosomeY
Orientationminus
Position2655467
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894957(C;C)
Make rs104894957(C;G)
OMIM480000
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104894957(C;C)
Alt rs104894957(C;C)
Reference rs104894957(G;G)
Significance 5
Disease 46
ClinVar info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
CLNHGVS NC_000024.9:g.2655467C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010392.1