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rs727503007

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503007(C;T)
Make rs727503007(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position70028006
GeneEDA
is asnp
is mentioned by
dbSNPrs727503007
ebirs727503007
HLIrs727503007
Exacrs727503007
Varsomers727503007
Maprs727503007
PheGenIrs727503007
hapmaprs727503007
1000 genomesrs727503007
hgdprs727503007
ensemblrs727503007
gopubmedrs727503007
geneviewrs727503007
scholarrs727503007
googlers727503007
pharmgkbrs727503007
gwascentralrs727503007
openSNPrs727503007
23andMers727503007
23andMe allrs727503007
SNP Nexus

SNPshotrs727503007
SNPdbers727503007
MSV3drs727503007
GWAS Ctlgrs727503007
Max Magnitude0
ClinVar
Risk rs727503007(T;T)
Alt rs727503007(T;T)
Reference rs727503007(C;C)
Significance Pathogenic
Disease Hypohidrotic ectodermal dysplasia
Variation info
Gene EDA
CLNDBN Hypohidrotic ectodermal dysplasia
Reversed 0
HGVS NC_000023.10:g.69247856C>T
CLNSRC
CLNACC RCV000150598.1,