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rs56160159

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs56160159(C;T)
Make rs56160159(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position56859851
GeneMAP3K1
is asnp
is mentioned by
dbSNPrs56160159
dbSNP (classic)rs56160159
ClinGenrs56160159
ebirs56160159
HLIrs56160159
Exacrs56160159
Gnomadrs56160159
Varsomers56160159
LitVarrs56160159
Maprs56160159
PheGenIrs56160159
Biobankrs56160159
1000 genomesrs56160159
hgdprs56160159
ensemblrs56160159
geneviewrs56160159
scholarrs56160159
googlers56160159
pharmgkbrs56160159
gwascentralrs56160159
openSNPrs56160159
23andMers56160159
SNPshotrs56160159
SNPdbers56160159
MSV3drs56160159
GWAS Ctlgrs56160159
Max Magnitude0
ClinVar
Risk rs56160159(T;T)
Alt rs56160159(T;T)
Reference Rs56160159(C;C)
Significance Probable-Pathogenic
Disease 46
Variation info
Gene MAP3K1
CLNDBN 46,XY sex reversal, type 6
Reversed 0
HGVS NC_000005.9:g.56155678C>T
CLNSRC
CLNACC RCV000197066.1,