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rs104894666

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894666(C;T)
Make rs104894666(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position2250667
GeneAMH, MIR4321
is asnp
is mentioned by
dbSNPrs104894666
ebirs104894666
HLIrs104894666
Exacrs104894666
Varsomers104894666
Maprs104894666
PheGenIrs104894666
hapmaprs104894666
1000 genomesrs104894666
hgdprs104894666
ensemblrs104894666
gopubmedrs104894666
geneviewrs104894666
scholarrs104894666
googlers104894666
pharmgkbrs104894666
gwascentralrs104894666
openSNPrs104894666
23andMers104894666
23andMe allrs104894666
SNP Nexus

SNPshotrs104894666
SNPdbers104894666
MSV3drs104894666
GWAS Ctlgrs104894666
Max Magnitude0
OMIM600957
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894666(T;T)
Alt rs104894666(T;T)
Reference rs104894666(C;C)
Significance Pathogenic
Disease Persistent mullerian duct syndrome
Variation info
Gene AMH MIR4321
CLNDBN Persistent mullerian duct syndrome, type I
Reversed 0
HGVS NC_000019.9:g.2250666C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009156.3,