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rs104894977

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894977(C;T)
Make rs104894977(T;T)
ReferenceGRCh38 38.1/141
ChromosomeY
Position2787600
GeneSRY
is asnp
is mentioned by
dbSNPrs104894977
ebirs104894977
HLIrs104894977
Exacrs104894977
Varsomers104894977
Maprs104894977
PheGenIrs104894977
hapmaprs104894977
1000 genomesrs104894977
hgdprs104894977
ensemblrs104894977
gopubmedrs104894977
geneviewrs104894977
scholarrs104894977
googlers104894977
pharmgkbrs104894977
gwascentralrs104894977
openSNPrs104894977
23andMers104894977
23andMe allrs104894977
SNP Nexus

SNPshotrs104894977
SNPdbers104894977
MSV3drs104894977
GWAS Ctlgrs104894977
Y Chromrs104894977
Max Magnitude0
OMIM480000
Desc
Variant0020
Relatedalso
ClinVar
Risk rs104894977(T;T)
Alt rs104894977(T;T)
Reference rs104894977(C;C)
Significance Pathogenic
Disease 46
Variation info
Gene SRY
CLNDBN 46,XY sex reversal, type 1
Reversed 1
HGVS NC_000024.9:g.2655641G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010407.3,