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rs267606654

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606654(G;T)
Make rs267606654(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position2251418
GeneAMH
is asnp
is mentioned by
dbSNPrs267606654
ebirs267606654
HLIrs267606654
Exacrs267606654
Varsomers267606654
Maprs267606654
PheGenIrs267606654
hapmaprs267606654
1000 genomesrs267606654
hgdprs267606654
ensemblrs267606654
gopubmedrs267606654
geneviewrs267606654
scholarrs267606654
googlers267606654
pharmgkbrs267606654
gwascentralrs267606654
openSNPrs267606654
23andMers267606654
23andMe allrs267606654
SNP Nexus

SNPshotrs267606654
SNPdbers267606654
MSV3drs267606654
GWAS Ctlgrs267606654
Max Magnitude0
ClinVar
Risk rs267606654(T;T)
Alt rs267606654(T;T)
Reference rs267606654(G;G)
Significance Pathogenic
Disease Persistent mullerian duct syndrome
Variation info
Gene AMH
CLNDBN Persistent mullerian duct syndrome, type I
Reversed 0
HGVS NC_000019.9:g.2251417G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009153.4,