Rs104894957

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894957(C;C)
Make rs104894957(C;G)
ReferenceGRCh38 38.1/141
ChromosomeY
Position2787426
GeneSRY
is asnp
is mentioned by
dbSNPrs104894957
Exacrs104894957
PheGenIrs104894957
nextbiors104894957
hapmaprs104894957
1000 genomesrs104894957
hgdprs104894957
ensemblrs104894957
gopubmedrs104894957
geneviewrs104894957
scholarrs104894957
googlers104894957
pharmgkbrs104894957
gwascentralrs104894957
openSNPrs104894957
23andMers104894957
23andMe allrs104894957
SNP Nexus

SNPshotrs104894957
SNPdbers104894957
MSV3drs104894957
Y Chromrs104894957
OMIM480000
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104894957(C;C)
Alt rs104894957(C;C)
Reference rs104894957(G;G)
Significance Pathogenic
Disease 46
Variation info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
HGVS NC_000024.9:g.2655467C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010392.1,