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rs727504901

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504901(A;G)
Make rs727504901(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154379688
GeneEMD
is asnp
is mentioned by
dbSNPrs727504901
ebirs727504901
HLIrs727504901
Exacrs727504901
Varsomers727504901
Maprs727504901
PheGenIrs727504901
hapmaprs727504901
1000 genomesrs727504901
hgdprs727504901
ensemblrs727504901
gopubmedrs727504901
geneviewrs727504901
scholarrs727504901
googlers727504901
pharmgkbrs727504901
gwascentralrs727504901
openSNPrs727504901
23andMers727504901
23andMe allrs727504901
SNP Nexus

SNPshotrs727504901
SNPdbers727504901
MSV3drs727504901
GWAS Ctlgrs727504901
Max Magnitude0
ClinVar
Risk rs727504901(G;G)
Alt rs727504901(G;G)
Reference rs727504901(A;A)
Significance Probable-Pathogenic
Disease Emery-Dreifuss muscular dystrophy
Variation info
Gene EMD
CLNDBN Emery-Dreifuss muscular dystrophy, X-linked
Reversed 0
HGVS NC_000023.10:g.153608048A>G
CLNSRC
CLNACC RCV000156286.1,