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rs727503011

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503011(C;T)
Make rs727503011(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position70035424
GeneEDA
is asnp
is mentioned by
dbSNPrs727503011
ebirs727503011
HLIrs727503011
Exacrs727503011
Varsomers727503011
Maprs727503011
PheGenIrs727503011
hapmaprs727503011
1000 genomesrs727503011
hgdprs727503011
ensemblrs727503011
gopubmedrs727503011
geneviewrs727503011
scholarrs727503011
googlers727503011
pharmgkbrs727503011
gwascentralrs727503011
openSNPrs727503011
23andMers727503011
23andMe allrs727503011
SNP Nexus

SNPshotrs727503011
SNPdbers727503011
MSV3drs727503011
GWAS Ctlgrs727503011
Max Magnitude0
ClinVar
Risk rs727503011(T;T)
Alt rs727503011(T;T)
Reference rs727503011(C;C)
Significance Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.69255274C>T
CLNSRC
CLNACC RCV000150607.1,