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rs387906788

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906788(C;C)
Make rs387906788(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position56856683
GeneMAP3K1
is asnp
is mentioned by
dbSNPrs387906788
ebirs387906788
HLIrs387906788
Exacrs387906788
Varsomers387906788
Maprs387906788
PheGenIrs387906788
hapmaprs387906788
1000 genomesrs387906788
hgdprs387906788
ensemblrs387906788
gopubmedrs387906788
geneviewrs387906788
scholarrs387906788
googlers387906788
pharmgkbrs387906788
gwascentralrs387906788
openSNPrs387906788
23andMers387906788
23andMe allrs387906788
SNP Nexus

SNPshotrs387906788
SNPdbers387906788
MSV3drs387906788
GWAS Ctlgrs387906788
Max Magnitude0
ClinVar
Risk rs387906788(C,G;C,G)
Alt rs387906788(C,G;C,G)
Reference rs387906788(T;T)
Significance Pathogenic
Disease 46
Variation info
Gene MAP3K1
CLNDBN 46,XY sex reversal, type 6
Reversed 0
HGVS NC_000005.9:g.56152510T>C; NC_000005.9:g.56152510T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023057.3, RCV000023058.2,