rs267606654

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs267606654(G;T)

Make rs267606654(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

2251418

Gene

AMH

is a	snp
is	mentioned by
dbSNP	rs267606654
dbSNP (classic)	rs267606654
ClinGen	rs267606654
ebi	rs267606654
HLI	rs267606654
Exac	rs267606654
Gnomad	rs267606654
Varsome	rs267606654
LitVar	rs267606654
Map	rs267606654
PheGenI	rs267606654
Biobank	rs267606654
1000 genomes	rs267606654
hgdp	rs267606654
ensembl	rs267606654
geneview	rs267606654
scholar	rs267606654
google	rs267606654
pharmgkb	rs267606654
gwascentral	rs267606654
openSNP	rs267606654
23andMe	rs267606654
SNPshot	rs267606654
SNPdbe	rs267606654
MSV3d	rs267606654
GWAS Ctlg	rs267606654

Max Magnitude

0

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,