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rs886039769

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039769(C;T)
Make rs886039769(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position124500686
GeneNR5A1
is asnp
is mentioned by
dbSNPrs886039769
dbSNP (classic)rs886039769
ClinGenrs886039769
ebirs886039769
HLIrs886039769
Exacrs886039769
Gnomadrs886039769
Varsomers886039769
LitVarrs886039769
Maprs886039769
PheGenIrs886039769
Biobankrs886039769
1000 genomesrs886039769
hgdprs886039769
ensemblrs886039769
geneviewrs886039769
scholarrs886039769
googlers886039769
pharmgkbrs886039769
gwascentralrs886039769
openSNPrs886039769
23andMers886039769
SNPshotrs886039769
SNPdbers886039769
MSV3drs886039769
GWAS Ctlgrs886039769
Max Magnitude0
ClinVar
Risk rs886039769(T;T)
Alt rs886039769(T;T)
Reference Rs886039769(C;C)
Significance Other
Disease 46
Variation info
Gene NR5A1
CLNDBN 46,XY sex reversal, type 3 46,XX sex reversal 4
Reversed 1
HGVS NC_000009.11:g.127262965G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000256210.1, RCV000490553.1,