rs886041854

Orientation

plus

Stabilized

plus

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

Chromosome

X

Position

154379544

Gene

EMD

is a	snp
is	mentioned by
dbSNP	rs886041854
dbSNP (classic)	rs886041854
ClinGen	rs886041854
ebi	rs886041854
HLI	rs886041854
Exac	rs886041854
Gnomad	rs886041854
Varsome	rs886041854
LitVar	rs886041854
Map	rs886041854
PheGenI	rs886041854
Biobank	rs886041854
1000 genomes	rs886041854
hgdp	rs886041854
ensembl	rs886041854
geneview	rs886041854
scholar	rs886041854
google	rs886041854
pharmgkb	rs886041854
gwascentral	rs886041854
openSNP	rs886041854
23andMe	rs886041854
SNPshot	rs886041854
SNPdbe	rs886041854
MSV3d	rs886041854
GWAS Ctlg	rs886041854

Max Magnitude

0

ClinVar
Risk	rs886041854(-;-)
Alt	rs886041854(-;-)
Reference	Rs886041854(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	EMD
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.153607904delC
CLNSRC
CLNACC	RCV000283932.1,