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rs387906751

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906751(A;C)
Make rs387906751(C;C)
ReferenceGRCh38 38.1/141
Chromosome10
Position4991861
GeneAKR1C2
is asnp
is mentioned by
dbSNPrs387906751
ebirs387906751
HLIrs387906751
Exacrs387906751
Varsomers387906751
Maprs387906751
PheGenIrs387906751
hapmaprs387906751
1000 genomesrs387906751
hgdprs387906751
ensemblrs387906751
gopubmedrs387906751
geneviewrs387906751
scholarrs387906751
googlers387906751
pharmgkbrs387906751
gwascentralrs387906751
openSNPrs387906751
23andMers387906751
23andMe allrs387906751
SNP Nexus

SNPshotrs387906751
SNPdbers387906751
MSV3drs387906751
GWAS Ctlgrs387906751
Max Magnitude0
ClinVar
Risk rs387906751(C;C)
Alt rs387906751(C;C)
Reference rs387906751(A;A)
Significance Pathogenic
Disease 46
Variation info
Gene AKR1C2
CLNDBN 46,XY sex reversal 8
Reversed 1
HGVS NC_000010.10:g.5034053T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000022969.3,